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1. Ruiz-Tovar J, Reguero-Callejas ME, Arano-Bermejo JI, González-Palacios F, Cabañas-Navarro L: [Mammary hamartoma]. Cir Esp; 2006 Mar;79(3):186-8
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  • [Title] [Mammary hamartoma].
  • [Transliterated title] Hamartoma mamario.
  • For many years, mammary hamartoma was considered to be an under-diagnosed disease.
  • Mammary hamartomas normally manifest as painless, mobile, palpable lumps without adherence to skin or muscle.
  • Because of the lack of cytological and architectural specificity of hamartomas, correlation between clinical manifestations, imaging techniques and histology is essential.
  • This report describes a case of an 11-cm mammary hamartoma in a 46-year-old woman.
  • [MeSH-major] Breast Diseases / pathology. Hamartoma / pathology

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  • (PMID = 16545287.001).
  • [ISSN] 0009-739X
  • [Journal-full-title] Cirugía española
  • [ISO-abbreviation] Cir Esp
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Spain
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2. Sardón O, Marhuenda C, Santiago M, Torán N, Korta J, Corcuera P, Barceló C, Pérez-Yarza EG: [Endobronchial chondromesenchymal hamartoma]. An Pediatr (Barc); 2010 Apr;72(4):263-6
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  • [Title] [Endobronchial chondromesenchymal hamartoma].
  • [Transliterated title] Hamartoma condromesenquimal endobronquial.
  • Among these tumours, endobronchial masses are even less common and, among benign tumours, inflammatory pseudotumours and hamartomas have the highest incidence in children.
  • We present the case of a 2.5-year-old girl with a left endobronchial chondromesenchymal hamartoma with obstruction of 90% of the bronchial lumen.
  • [MeSH-major] Bronchial Diseases. Hamartoma

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  • [Copyright] 2009 Asociación Española de Pediatría. Published by Elsevier Espana. All rights reserved.
  • (PMID = 20206588.001).
  • [ISSN] 1695-9531
  • [Journal-full-title] Anales de pediatría (Barcelona, Spain : 2003)
  • [ISO-abbreviation] An Pediatr (Barc)
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Spain
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3. Messina MP, Rauktys A, Lee L, Dabora SL: Tuberous sclerosis preclinical studies: timing of treatment, combination of a rapamycin analog (CCI-779) and interferon-gamma, and comparison of rapamycin to CCI-779. BMC Pharmacol; 2007 Nov 06;7:14
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  • BACKGROUND: Tuberous Sclerosis Complex (TSC) is an autosomal dominant hamartoma disorder with variable expression for which treatment options are limited.
  • Rapamycin (also known as sirolimus), an mTOR inhibitor, has been shown to reduce disease severity in rodent models of TSC and is currently being evaluated in clinical trials in human populations.
  • A high-expressing IFN-gamma allele has been associated with reduced disease severity in human TSC patients and it has been shown in mouse models that treatment with exogenous IFN-gamma reduces disease severity.
  • As long as treatment is given after lesions arise, altering the time period during which treatment was given did not significantly impact the effect of the treatment on disease severity.

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  • [Cites] Hum Genet. 2000 Aug;107(2):97-114 [11030407.001]
  • [Cites] Am J Hum Genet. 2002 Oct;71(4):750-8 [12192641.001]
  • [Cites] Cell. 2001 May 4;105(3):357-68 [11348592.001]
  • [Cites] Oncogene. 2000 Dec 27;19(56):6680-6 [11426655.001]
  • [Cites] J Clin Oncol. 2004 Mar 1;22(5):909-18 [14990647.001]
  • [Cites] J Clin Oncol. 2004 Jun 15;22(12):2336-47 [15136596.001]
  • [Cites] J Clin Oncol. 2004 Jul 15;22(14):2954-63 [15254063.001]
  • [Cites] Invest New Drugs. 2004 Nov;22(4):427-35 [15292713.001]
  • [Cites] Am J Hum Genet. 1996 Aug;59(2):400-6 [8755927.001]
  • [Cites] J Clin Pharmacol. 1997 May;37(5):405-15 [9156373.001]
  • [Cites] Pharmacotherapy. 1997 Nov-Dec;17(6):1148-56 [9399599.001]
  • [Cites] Am J Pathol. 1997 Dec;151(6):1639-47 [9403714.001]
  • [Cites] Clin Pharmacol Ther. 1998 Jan;63(1):48-53 [9465841.001]
  • [Cites] Transplant Proc. 1998 Aug;30(5):2185-8 [9723435.001]
  • [Cites] J Clin Invest. 1999 Sep;104(6):687-95 [10491404.001]
  • [Cites] Nat Genet. 2005 Jan;37(1):19-24 [15624019.001]
  • [Cites] Pediatr Res. 2005 Jan;57(1):67-75 [15557109.001]
  • [Cites] Genes Chromosomes Cancer. 2005 Mar;42(3):213-27 [15578690.001]
  • [Cites] Curr Opin Genet Dev. 2005 Feb;15(1):69-76 [15661536.001]
  • [Cites] J Clin Oncol. 2005 Aug 10;23(23):5314-22 [15955899.001]
  • [Cites] J Clin Oncol. 2005 Aug 10;23(23):5386-403 [15983388.001]
  • [Cites] J Clin Oncol. 2005 Aug 10;23(23):5347-56 [15983389.001]
  • [Cites] J Clin Oncol. 2005 Aug 10;23(23):5294-304 [15998902.001]
  • [Cites] Ann Neurol. 2006 Mar;59(3):490-8 [16453317.001]
  • [Cites] Genes Chromosomes Cancer. 2006 Oct;45(10):933-44 [16845661.001]
  • [Cites] N Engl J Med. 2007 May 31;356(22):2271-81 [17538086.001]
  • [Cites] Nat Biotechnol. 2001 Oct;19(10):940-5 [11581659.001]
  • [Cites] Nat Cell Biol. 2002 Sep;4(9):699-704 [12172555.001]
  • [Cites] Am J Hum Genet. 2001 Jan;68(1):64-80 [11112665.001]
  • (PMID = 17986349.001).
  • [ISSN] 1471-2210
  • [Journal-full-title] BMC pharmacology
  • [ISO-abbreviation] BMC Pharmacol.
  • [Language] eng
  • [Grant] United States / NIDDK NIH HHS / DK / R01 DK066366; United States / NIDDK NIH HHS / DK / R01DK066366
  • [Publication-type] Comparative Study; Journal Article; Research Support, N.I.H., Extramural
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Antineoplastic Agents; 0 / Antiviral Agents; 624KN6GM2T / temsirolimus; 82115-62-6 / Interferon-gamma; W36ZG6FT64 / Sirolimus
  • [Other-IDs] NLM/ PMC2213639
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4. Díaz-Pérez JA, García-Ramírez CA, García-Vera JA, Melo-Uribe MA, Uribe CJ: [Rhabdomyomatous mesenchymal hamartoma]. Actas Dermosifiliogr; 2008 Jul-Aug;99(6):474-6
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  • [Title] [Rhabdomyomatous mesenchymal hamartoma].
  • [Transliterated title] Hamartoma mesenquimal rabdomiomatoso.
  • Rhabdomyomatous mesenchymal hamartoma is an extremely rare congenital lesion, and very few cases have been reported even though its macroscopic and microscopic features make diagnosis easy.
  • The mass was surgically removed, and rhabdomyomatous mesenchymal hamartoma was diagnosed.
  • [MeSH-major] Hamartoma / congenital. Skin Diseases / congenital

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  • (PMID = 18558056.001).
  • [ISSN] 0001-7310
  • [Journal-full-title] Actas dermo-sifiliográficas
  • [ISO-abbreviation] Actas Dermosifiliogr
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Spain
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5. Gockel I, Oberholzer K, Corinth C, Seifert JK, Junginger TH: [Hamartoma of the duodenum]. Dtsch Med Wochenschr; 2005 Jul 8;130(27):1637-40
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  • [Title] [Hamartoma of the duodenum].
  • [Transliterated title] Das Hamartom des Duodenums. Eine seltene Indikation zur partiellen Duodenopankreatektomie.
  • The histological examination of the resectate showed -- besides a chronically fibrosing pancreatitis -- a hamartoma of the duodenal wall.
  • CONCLUSION: Besides the endoscopic removal of a hamartoma of the duodenum a surgical transduodenal resection represents the most frequently applied procedure.
  • [MeSH-major] Duodenal Diseases / surgery. Hamartoma / surgery. Pancreaticoduodenectomy / methods

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  • (PMID = 15988662.001).
  • [ISSN] 0012-0472
  • [Journal-full-title] Deutsche medizinische Wochenschrift (1946)
  • [ISO-abbreviation] Dtsch. Med. Wochenschr.
  • [Language] ger
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Germany
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6. Gupta N, Singh N, Sarangi S, Dalmia S, Mittal S: Fetal cardiac rhabdomyoma with maternal tuberous sclerosis complicating pregnancy. Arch Gynecol Obstet; 2008 Aug;278(2):169-70
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  • INTRODUCTION: Tuberous sclerosis is an autosomal dominant disorder of hamartoma formation that can manifest as cardiac or central nervous system lesions and adversely affect maternal and fetal outcome.


7. Cuartero V, López J, Carrero J, Nevado M: [Retrorectal cystic hamartoma (tailgut cyst): radiologic and pathologic findings]. Radiologia; 2008 Sep-Oct;50(5):430-3
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  • [Title] [Retrorectal cystic hamartoma (tailgut cyst): radiologic and pathologic findings].
  • [Transliterated title] Hamartoma quístico retrorrectal: hallazgos radiopatológicos.
  • Cystic hamartoma is a rare congenital lesion that presents as a presacral mass.
  • It is difficult to distinguish the imaging appearance of cystic hamartoma from that of many other presacral cysts; therefore, histologic analysis is essential for the definitive diagnosis.
  • [MeSH-major] Hamartoma / diagnosis. Pregnancy Complications / diagnosis. Rectal Neoplasms / diagnosis

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  • (PMID = 19055922.001).
  • [ISSN] 0033-8338
  • [Journal-full-title] Radiología
  • [ISO-abbreviation] Radiologia
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article; Review
  • [Publication-country] Spain
  • [Number-of-references] 7
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8. Toledano Muñoz A, Navarro Cunchillos M, García Simal M, Galindo Campillo AN: [Nasal hamartoma]. Acta Otorrinolaringol Esp; 2010 Mar-Apr;61(2):163-5
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  • [Title] [Nasal hamartoma].
  • [Transliterated title] Hamartoma nasal.
  • Nasal hamartoma is a rare lesion characterized by a mix of several tissue types.
  • We report the case of a 35-year-old woman presenting hamartoma in the posterosuperior part of the right nasal cavity.
  • Hamartomas must be included in the differential diagnostic of unilateral nasal masses, along with inverted papillomas and malignant tumours.
  • [MeSH-major] Hamartoma. Nose Diseases

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  • [Copyright] Copyright 2008 Elsevier España, S.L. All rights reserved.
  • (PMID = 19818429.001).
  • [ISSN] 1988-3013
  • [Journal-full-title] Acta otorrinolaringológica española
  • [ISO-abbreviation] Acta Otorrinolaringol Esp
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article; Review
  • [Publication-country] Spain
  • [Number-of-references] 6
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9. Dorfmüller G, Fohlen M, Bulteau C, Delalande O: [Surgical disconnection of hypothalamic hamartomas]. Neurochirurgie; 2008 May;54(3):315-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Surgical disconnection of hypothalamic hamartomas].
  • [Transliterated title] Déconnexion chirurgicale des hamartomes hypothalamiques.
  • BACKGROUND AND PURPOSE: Surgical resection of hypothalamic hamartomas (HHs) associated with drug-resistant gelastic epilepsy carries a considerable risk of neurological and endocrine morbidity.
  • The hamartoma was disconnected using a microsurgical pterional approach of those lesions extending from the hypothalamic floor downward into the interpeduncular cistern.
  • According to the different topographic features of the HHs, for which we have recently proposed a classification into four subtypes, the intraventricularly located hamartoma had the best prognosis following endoscopic disconnection.
  • [MeSH-major] Hamartoma / surgery. Hypothalamic Diseases / surgery. Neurosurgical Procedures

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  • (PMID = 18452954.001).
  • [ISSN] 0028-3770
  • [Journal-full-title] Neuro-Chirurgie
  • [ISO-abbreviation] Neurochirurgie
  • [Language] fre
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] France
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10. Luba M, Bossowski A, Kulikowska J, Urban M, Szarras-Czapnik M, Rutkowski R, Parol T, Gasiorek T, Sawicka B, Skrzydło M: [Precocious puberty due to hypothalamic hamartoma]. Pediatr Endocrinol Diabetes Metab; 2008;14(4):257-61
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  • [Title] [Precocious puberty due to hypothalamic hamartoma].
  • [Transliterated title] Przedwczesne dojrzewanie płciowe w przebiegu guza hamartoma podwzgórza.
  • Appearance of the precocious puberty symptoms in early childhood or pre-school period indicate that also it could be caused by organic disorder of the central nervous system.
  • In conclusion, we aspired to notice that the pharmacological treatment of hypothalamic hamartoma may be safe and effective.
  • [MeSH-major] Hamartoma / complications. Hamartoma / diagnosis. Hypothalamic Diseases / complications. Hypothalamic Diseases / diagnosis. Puberty, Precocious / etiology

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  • (PMID = 19239796.001).
  • [ISSN] 2081-237X
  • [Journal-full-title] Pediatric endocrinology, diabetes, and metabolism
  • [ISO-abbreviation] Pediatr Endocrinol Diabetes Metab
  • [Language] pol
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Poland
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11. Rojas Llimpe F, Di Fabio F, Ercolani G, Giampalma E, Serra C, Castellucci P, Pini S, Mutri V, Golfieri R, Pinto C, Martoni A: Presurgical comparative imaging evaluation in patients with colorectal cancer liver metastasis (PROMETEO Study). J Clin Oncol; 2009 May 20;27(15_suppl):e15010
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  • Five lesions at pathological examination were non-metastasis (1 hamartoma, 1 steatosis, 1 giant-cell reaction, 2 necrosis).

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  • (PMID = 27964437.001).
  • [ISSN] 1527-7755
  • [Journal-full-title] Journal of clinical oncology : official journal of the American Society of Clinical Oncology
  • [ISO-abbreviation] J. Clin. Oncol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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12. Di Blasi A, Boscaino A, De Dominicis G, Marino-Marsilia G: [Splenic hamartoma]. Pathologica; 2005 Jun;97(3):124-9
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  • [Title] [Splenic hamartoma].
  • [Transliterated title] Amartoma splenico.
  • The Authors present a case of Splenic Hamartoma.
  • The Authors judge this complex picture as indicative of a Splenic Hamartoma with a peculiar lobular-nodular pattern that seems to coincide with the recently described SANT: Sclerosing Angiomatoid Nodular Transformation of the spleen.
  • It is also emphasized the Hamartoma's great variety of morphologic patterns derived from the preponderant growth of one or another of several histologic components.
  • The Authors discuss the differential diagnosis of Splenic Hamartoma with other lesions as haemangiomas and inflammatory pseudotumor.
  • [MeSH-major] Hamartoma / pathology. Splenic Neoplasms / pathology

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  • (PMID = 16259278.001).
  • [ISSN] 0031-2983
  • [Journal-full-title] Pathologica
  • [ISO-abbreviation] Pathologica
  • [Language] ita
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Italy
  • [Chemical-registry-number] 0 / Actins; 0 / Antigens, CD; 0 / Biomarkers, Tumor; 0 / Collagen Type IV; 0 / Neoplasm Proteins; 0 / Vimentin
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13. Hahn CH, Munch-Petersen HR: [Leiomyomatous hamartoma at base of tongue]. Ugeskr Laeger; 2010 Mar 1;172(9):710-1
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  • [Title] [Leiomyomatous hamartoma at base of tongue].
  • [Transliterated title] Leiomyomatøst hamartom ved tungebasis.
  • We report a case of a leiomyomatous hamartoma located in the midline of the base of the tongue.
  • [MeSH-major] Hamartoma. Tongue Neoplasms

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  • (PMID = 20199749.001).
  • [ISSN] 1603-6824
  • [Journal-full-title] Ugeskrift for laeger
  • [ISO-abbreviation] Ugeskr. Laeg.
  • [Language] dan
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Denmark
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14. Vega Menéndez D, Quintáns Rodríguez A, Hernández Granados P, Nevado Santos M, García Sabrido JL, Rueda Orgaz JA, Ochando F, Ojeda Pérez F, Loinaz C: [Tailgut cysts]. Cir Esp; 2008 Feb;83(2):53-60
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Transliterated title] Hamartomas quísticos retrorrectales.
  • Retrorectal cystic hamartomas (tailgut cysts) are rare congenital lesions thought to arise from remnants of the embryonic postanal gut.
  • [MeSH-major] Cysts. Hamartoma. Rectal Diseases

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  • (PMID = 18261408.001).
  • [ISSN] 0009-739X
  • [Journal-full-title] Cirugía española
  • [ISO-abbreviation] Cir Esp
  • [Language] spa
  • [Publication-type] Case Reports; Comparative Study; English Abstract; Journal Article; Review
  • [Publication-country] Spain
  • [Number-of-references] 64
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15. Lorenzoni PJ, Lange MC, Kay CS, Silvado CE, Scola RH, Werneck LC: [Fibrolipomatous hamartoma of the median nerve: case report]. Arq Neuropsiquiatr; 2005 Sep;63(3B):881-4
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Fibrolipomatous hamartoma of the median nerve: case report].
  • [Transliterated title] Hamartoma fibrolipomatoso de nervo mediano: relato de caso.
  • Fibrolipomatous hamartoma is a rare benign neoplasm that in some cases is associated with macrodactylia.
  • Investigation with X-ray, ultrasonography, electrodiagnosis, magnetic resonance image of the left wrist and hand showed carpal tunnel syndrome with macrodactylia by fibrolipomatous hamartoma of the median nerve.
  • [MeSH-major] Carpal Tunnel Syndrome / etiology. Hamartoma / complications. Median Nerve / pathology. Median Neuropathy / pathology

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  • (PMID = 16258677.001).
  • [ISSN] 0004-282X
  • [Journal-full-title] Arquivos de neuro-psiquiatria
  • [ISO-abbreviation] Arq Neuropsiquiatr
  • [Language] por
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Brazil
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16. Plett D, Reineke U, Hamberger U, Sudhoff H: [Hamartoma : a rare nasopharyngeal pathology as a cause of nasal obstruction]. HNO; 2009 Dec;57(12):1329-32
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Hamartoma : a rare nasopharyngeal pathology as a cause of nasal obstruction].
  • [Transliterated title] Das Hamartom : Eine seltene nasopharyngeale Pathologie als Ursache einer Nasenatmungsbehinderung.
  • Histologic examination showed a respiratory epithelial adenomatoid hamartoma.
  • [MeSH-major] Hamartoma / diagnosis. Nasal Obstruction / etiology. Nasopharyngeal Diseases / diagnosis

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  • (PMID = 19777171.001).
  • [ISSN] 1433-0458
  • [Journal-full-title] HNO
  • [ISO-abbreviation] HNO
  • [Language] ger
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Germany
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17. Adam MP, Abramowsky CR, Brady AN, Coleman K, Todd NW: Rhabdomyomatous hamartomata of the pharyngeal region with bilateral microtia and aural atresia: a new association? Birth Defects Res A Clin Mol Teratol; 2007 Mar;79(3):242-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Rhabdomyomatous hamartomata of the pharyngeal region with bilateral microtia and aural atresia: a new association?
  • Rhabdomyomatous hamartomata containing salivary tissue, situated bilaterally and symmetrically simulating the palatine (faucial) tonsils, has apparently not been reported.
  • Histopathologic studies demonstrated rhabdomyomatous hamartomata containing salivary and striated muscle tissue in place of the palatine tonsils.
  • Again, histopathologic studies of the tissue submitted as "tonsil" demonstrated rhabdomyomatous hamartomata containing salivary and muscle tissue.
  • CONCLUSIONS: We hypothesize that the findings of bilateral microtia with aural atresia and rhabdomyomatous hamartomata containing salivary and muscle tissue in the area of the palatine tonsils may represent a newly recognized association, which may have a teratogenic and/or genetic etiology.
  • [MeSH-major] Ear Canal / abnormalities. Ear, External / abnormalities. Hamartoma / complications. Pharyngeal Diseases / complications

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  • (PMID = 17177266.001).
  • [ISSN] 1542-0752
  • [Journal-full-title] Birth defects research. Part A, Clinical and molecular teratology
  • [ISO-abbreviation] Birth Defects Res. Part A Clin. Mol. Teratol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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18. García-Toral R, Villarreal-Zaunbos MA, Vásquez-Fernández F, Prieto-Murguía EG, Aguilar-Padilla L: [Pulmonary hamartoma. A case report]. Gac Med Mex; 2007 Jul-Aug;143(4):345-7
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  • [Title] [Pulmonary hamartoma. A case report].
  • [Transliterated title] Hamartoma pulmonar. Informe de un caso.
  • A 71-years-old man presented with an incidentally finding of a tumor in the left pulmonary apex that measured approximately 4.5 cm of diameter.
  • The final diagnosis was hamartoma of the lung.
  • [MeSH-major] Hamartoma. Lung Neoplasms
  • [MeSH-minor] Aged. Biopsy. Bronchoscopy. Carcinoma, Squamous Cell / diagnosis. Diagnosis, Differential. Disease Progression. Humans. Lung / pathology. Male. Radiography, Thoracic. Thoracotomy. Time Factors. Tomography, X-Ray Computed

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  • (PMID = 17969844.001).
  • [ISSN] 0016-3813
  • [Journal-full-title] Gaceta médica de México
  • [ISO-abbreviation] Gac Med Mex
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Mexico
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19. Hes O, Sůvová B, Hlavácková M, Giebel P, Kinkor Z: [Harmatoma of the breast--case report]. Ceska Gynekol; 2006 Jul;71(4):351-4
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  • [Transliterated title] Hamartom prsu--kazuistika.
  • OBJECTIVE: To describe rare hamartoma of the breast in a 31-year-old female.
  • Subsequent histological examination revealed breast hamartoma.
  • The patient is alive and well without signs of disease one year after excision.
  • CONCLUSION: Hamartoma of the breast is a rare benign tumor.

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  • (PMID = 16956054.001).
  • [ISSN] 1210-7832
  • [Journal-full-title] Ceska gynekologie
  • [ISO-abbreviation] Ceska Gynekol
  • [Language] CZE
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Czech Republic
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20. Reichenbach-Klinke E, Miksch T, Orner R, Bergelt S, Sterk P: [Hamartoma of the duodenum: a rare cause of gastrointestinal bleeding]. Chirurg; 2010 Dec;81(12):1115-7
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  • [Title] [Hamartoma of the duodenum: a rare cause of gastrointestinal bleeding].
  • [Transliterated title] Hamartom des Duodenums: Seltene Ursache einer gastrointestinalen Blutung.
  • The 10 cm long tumor was resected transduodenally by open surgery and the histological examination revealed it to be a hamartoma.
  • [MeSH-major] Duodenal Neoplasms / diagnosis. Duodenal Neoplasms / surgery. Gastrointestinal Hemorrhage / etiology. Hamartoma / diagnosis. Hamartoma / surgery. Intestinal Polyps / diagnosis. Intestinal Polyps / surgery

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  • (PMID = 20428835.001).
  • [ISSN] 1433-0385
  • [Journal-full-title] Der Chirurg; Zeitschrift für alle Gebiete der operativen Medizen
  • [ISO-abbreviation] Chirurg
  • [Language] ger
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Germany
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21. Morales OL, Valencia Mde L, Gómez C, Pérez Mdel P, Sanín E, Vásquez LM: [Chest wall mesenchymal hamartoma: a case report]. Biomedica; 2010 Jan-Mar;30(1):10-4
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  • [Title] [Chest wall mesenchymal hamartoma: a case report].
  • [Transliterated title] Hamartoma mesenquimatoso de la pared torácica: presentación de un caso.
  • Chest wall mesenchymal hamartoma is an extremely rare benign tumor.
  • Herein, a case is described of a four month old infant with diagnosis of chest wall mesenchymal hamartoma, manifested at birth.
  • [MeSH-major] Hamartoma. Thoracic Wall

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  • (PMID = 20890544.001).
  • [ISSN] 0120-4157
  • [Journal-full-title] Biomédica : revista del Instituto Nacional de Salud
  • [ISO-abbreviation] Biomedica
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Colombia
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22. Ferreira D, Almeida J, Parente B, Moura E Sá J: [Complete resection of endobronchial hamartomas via bronchoscopic techniques, electrosurgery by Argon plasma and laser]. Rev Port Pneumol; 2007 Sep-Oct;13(5):711-9
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  • [Title] [Complete resection of endobronchial hamartomas via bronchoscopic techniques, electrosurgery by Argon plasma and laser].
  • [Transliterated title] Ressecção completa de hamartomas endobrônquicos por técnicas broncoscópicas, electrocirurgia por argon plasma e laser Nd-YAG.
  • Hamartomas are benign neoplasms often located in lung and frequently asymptomatic.
  • About 1.4-20% of hamartomas have endobronchial location and can be symptomatic due to airway obstruction.
  • Traditionally, surgical resection has been considered the standard of care for endobronchial hamartoma.
  • We report two cases of endobronchial hamartomas, each diagnosed and definitively treated with bronchoscopic techniques.
  • Follow-up bronchoscopic examinations excluded residual or recurrent disease.
  • [MeSH-major] Bronchial Diseases / surgery. Bronchoscopy. Electrosurgery. Hamartoma / surgery. Laser Therapy

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  • (PMID = 17962889.001).
  • [ISSN] 0873-2159
  • [Journal-full-title] Revista portuguesa de pneumologia
  • [ISO-abbreviation] Rev Port Pneumol
  • [Language] por
  • [Publication-type] Case Reports; English Abstract; Journal Article; Review
  • [Publication-country] Portugal
  • [Number-of-references] 10
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23. Agabiti S, Gurrera A, Amico P, Vasquez E, Magro G: [Mammary hamartoma with atypical stromal cells: a potential diagnostic dilemma]. Pathologica; 2007 Dec;99(6):434-7
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  • [Title] [Mammary hamartoma with atypical stromal cells: a potential diagnostic dilemma].
  • [Transliterated title] Amartoma mammario con cellule stromali atipiche: un potenziale allarme diagnostico per il patologo.
  • Hamartoma of the breast is a pseudotumoural lesion that does not usually pose diagnostic problems for the pathologist.
  • Although atypical stromal cell (ASCs) can be encountered in several benign and malignant breast lesions, their occurrence in hamartoma has not been reported to date.
  • The authors report a case of breast hamartoma containing numerous atypical mono- or multinucleated stromal cells within the fibro-fatty component.
  • [MeSH-major] Breast Diseases / diagnosis. Hamartoma / diagnosis

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  • (PMID = 18416336.001).
  • [ISSN] 0031-2983
  • [Journal-full-title] Pathologica
  • [ISO-abbreviation] Pathologica
  • [Language] ita
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Italy
  • [Chemical-registry-number] 0 / Antigens, CD34; 0 / Biomarkers; 0 / Vimentin
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24. Lee A, Heidary N, Altiner A, Votava H, Kamino H, Sanchez M: Neurovascular hamartoma. Dermatol Online J; 2009;15(8):21
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  • [Title] Neurovascular hamartoma.
  • Histopathological analyses of the biopsy specimens was consistent with a rare entity known as neurovascular hamartoma.
  • This uncommon lesion has been reported in two publications, either as a possible marker of the malignant rhabdoid tumor or as a hamartomatous tongue lesion in children.
  • [MeSH-major] Hamartoma / pathology. Skin Diseases / pathology

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  • (PMID = 19891929.001).
  • [ISSN] 1087-2108
  • [Journal-full-title] Dermatology online journal
  • [ISO-abbreviation] Dermatol. Online J.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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25. Gleizal A, Chekaroua K, Beziat JL, Delay E: [Evolution of sebaceous hamartoma: prospective pathologic study illustrated with a voluminous ear location]. Ann Chir Plast Esthet; 2005 Dec;50(6):739-42
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  • [Title] [Evolution of sebaceous hamartoma: prospective pathologic study illustrated with a voluminous ear location].
  • [Transliterated title] Devenir des hamartomes sébacés: une étude anatomopathologigue prospective illustrée par un cas volumineux de la région auriculaire.
  • After an exeresis of a sebaceous hamartoma of retroauricular area, histologic examination showed a trichoblastoma mimicking a basal cell carcinoma.
  • So we realized a retrospective study with histologic examination of 24 cases of basal cell carcinoma after hamartoma.
  • So the study goes in the same direction of the world literature: hamartoma have a minimal risk of basal cell carcinoma transformation.
  • [MeSH-major] Carcinoma, Basal Cell / pathology. Hamartoma / pathology. Hamartoma / surgery. Sebaceous Gland Diseases / pathology. Sebaceous Gland Diseases / surgery

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  • (PMID = 16153762.001).
  • [ISSN] 0294-1260
  • [Journal-full-title] Annales de chirurgie plastique et esthétique
  • [ISO-abbreviation] Ann Chir Plast Esthet
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
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26. Krichen Makni S, Mnif Hachicha L, Ellouze S, Mnif M, Khabir A, Ketata H, Abid M, Sellami Boudawara T: [Feminizing testicular syndrome with multiple hamartomas and bilateral paratesticular leiomyomas]. Rev Med Interne; 2005 Dec;26(12):980-3
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  • [Title] [Feminizing testicular syndrome with multiple hamartomas and bilateral paratesticular leiomyomas].
  • [Transliterated title] Syndrome du testicule féminisant associé à des hamartomes multiples et à des léiomyomes paratesticulaires bilatéraux.
  • The testis were immature; they showed bilateral leiomyoma of the tunica albuginea and multiple hamartomas on the right side.
  • CONCLUSION: Benign tumors are developped in 80% of cases of TF and they are generally hamartomatous nodules of testis.
  • Association of paratesticular leiomyoma to synchronous hamartoma has never been described, its histogenesis is discussed.

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  • (PMID = 16236398.001).
  • [ISSN] 0248-8663
  • [Journal-full-title] La Revue de medecine interne
  • [ISO-abbreviation] Rev Med Interne
  • [Language] FRE
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
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27. Ammor A, Margi M, Lamalmi N, Oulahyane R, Malihy A, Cherkaoui A, Bouhafs A, Kaddouri N, Abdelhak M, Benhmamouch MN: [Mesenchymal hamartoma of the liver in a child: a case report]. Arch Pediatr; 2009 Jul;16(7):1033-6
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  • [Title] [Mesenchymal hamartoma of the liver in a child: a case report].
  • [Transliterated title] Hamartome du foie chez l'enfant : à propos d'un nouveau cas.
  • Mesenchymal hamartoma of the liver is a rare, benign tumor that presents mostly before the age of 2 years.
  • We present the case of a 2.5-year-old female patient who had a large cystic mass of the liver of which the hamartomatous nature was confirmed by the pathological examination of the surgical specimen.
  • [MeSH-major] Hamartoma / diagnosis. Liver Diseases / diagnosis

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  • (PMID = 19428226.001).
  • [ISSN] 1769-664X
  • [Journal-full-title] Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie
  • [ISO-abbreviation] Arch Pediatr
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
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28. Giunippero A, Maya AM, Gallo A, Bazzana MS, Cosentino V, Aulet FJ: [Mesenchymal hamartoma of the liver in an elderly man]. Medicina (B Aires); 2009;69(5):554-6
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  • [Title] [Mesenchymal hamartoma of the liver in an elderly man].
  • [Transliterated title] Hamartoma mesenquimatoso hepático en un anciano.
  • The mesenchymal hamartoma of the liver is a non frequent benign tumor with a ductal plate malformation, consisting of myxoid mesenchymal tissue and abnormal bile ducts in different proportion.
  • We present the case of an elder 87 year old male who presented a 20 cm mesenchymal hamartoma liver cyst.
  • [MeSH-major] Hamartoma / diagnosis. Liver Diseases / diagnosis

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  • (PMID = 19897442.001).
  • [ISSN] 0025-7680
  • [Journal-full-title] Medicina
  • [ISO-abbreviation] Medicina (B Aires)
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Argentina
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29. Martínez Quesada M, Trujillo Berraquero F, Almendro Delia M, Hidalgo Urbano R, Cruz Fernández JM: [Cardiac hamartoma. Case report and literature review]. Rev Esp Cardiol; 2005 Apr;58(4):450-2
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  • [Title] [Cardiac hamartoma. Case report and literature review].
  • [Transliterated title] Hamartoma intracardíaco. Caso clínico y revisión de la bibliografía.
  • They are sometimes an incidental finding in an asymptomatic patient.
  • The pathologic diagnosis was hamartoma of mature cardiac myocytes.
  • [MeSH-major] Hamartoma / diagnosis. Heart Diseases / diagnosis

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  • (PMID = 15847741.001).
  • [ISSN] 0300-8932
  • [Journal-full-title] Revista española de cardiología
  • [ISO-abbreviation] Rev Esp Cardiol
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article; Review
  • [Publication-country] Spain
  • [Number-of-references] 13
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30. Starska K, Lukomski M, Ratyńska M: [Rare case of a respiratory epithelial adenomatoid hamartoma of the nasal cavity, maxillary sinus et ethmoid sinuses: a clinicopathologic study]. Otolaryngol Pol; 2005;59(3):421-4
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  • [Title] [Rare case of a respiratory epithelial adenomatoid hamartoma of the nasal cavity, maxillary sinus et ethmoid sinuses: a clinicopathologic study].
  • [Transliterated title] Respiratory epithelial adenomatoid hamartoma jamy nosa, zatoki szczekowej i zatok sitowych: kliniczno-histopatologiczny opis przypadku.
  • A case of the respiratory epithelial adenomatoid hamartoma of the nasal cavity, maxillary sinus and ethmoid sinuses for the first time in the polish literature was reported.
  • [MeSH-major] Ethmoid Sinus. Hamartoma / diagnosis. Maxillary Sinus. Nasal Cavity / pathology. Paranasal Sinus Diseases / diagnosis. Paranasal Sinus Diseases / surgery

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  • (PMID = 16117401.001).
  • [ISSN] 0030-6657
  • [Journal-full-title] Otolaryngologia polska = The Polish otolaryngology
  • [ISO-abbreviation] Otolaryngol Pol
  • [Language] pol
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Poland
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31. Smit R, Gregorini D, Beltrán R, Martorelli J, Granada G, Lespi P: [Retrorectal cyst hamartoma: report of a pediatric case]. Arch Argent Pediatr; 2010 Jun;108(3):e82-5
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  • [Title] [Retrorectal cyst hamartoma: report of a pediatric case].
  • [Transliterated title] Hamartoma quístico retrorrectal: presentación de un caso pediátrico.
  • The retrorectal hamartoma cyst or retrorectal cyst is an uncommon congenital lesion.
  • [MeSH-major] Hamartoma. Rectal Diseases

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  • (PMID = 20544128.001).
  • [ISSN] 1668-3501
  • [Journal-full-title] Archivos argentinos de pediatría
  • [ISO-abbreviation] Arch Argent Pediatr
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Argentina
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32. Biedroń A, Steczkowska M, Gergont A, Kroczka S: [Course of gelastic epilepsy in a boy with non operated hypothalamic hamartoma]. Przegl Lek; 2010;67(11):1217-22
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  • [Title] [Course of gelastic epilepsy in a boy with non operated hypothalamic hamartoma].
  • [Transliterated title] Przebieg padaczki z napadami smiechu u dziecka z nie leczonym chirurgicznie hamartoma podwzgórza.
  • BACKGROUND: Gelastic epilepsy is usually symptomatic and most often associated with hypothalamic hamartoma.
  • AIM OF THE STUDY: Presentation of the experience from 5-year observation of the patient with gelastic epilepsy and hypothalamic hamartoma and comparison of this observation with previously reported in the literature with special attention to modern surgical treatment techniques.
  • Analysis of the literature concerning the surgical treatment in the patients with drug resistant gelastic epilepsy and hypothalamic hamartoma indicates the need of further studies in this area to establish qualification criteria for each type of surgical technique in order to minimize the risk of operative complications.
  • [MeSH-major] Epilepsies, Partial / diagnosis. Epilepsies, Partial / etiology. Hamartoma / complications. Hamartoma / diagnosis. Hypothalamic Diseases / complications. Hypothalamic Diseases / diagnosis

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  • (PMID = 21442980.001).
  • [ISSN] 0033-2240
  • [Journal-full-title] Przegla̧d lekarski
  • [ISO-abbreviation] Prz. Lek.
  • [Language] pol
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Poland
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33. Goulis DG, Iliadou PK, Papanicolaou A, Georgiou I, Chatzikyriakidou A, Gerou S, Bondis IN, Papadimas I: R831X mutation of the androgen receptor gene in an adolescent with complete androgen insensitivity syndrome and bilateral testicular hamartomata. Hormones (Athens); 2006 Jul-Sep;5(3):200-4
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  • [Title] R831X mutation of the androgen receptor gene in an adolescent with complete androgen insensitivity syndrome and bilateral testicular hamartomata.
  • The pathology report was that of "hamartomatous testes" and associated paratesticular leiomyoma.
  • [MeSH-major] Androgen-Insensitivity Syndrome / complications. Androgen-Insensitivity Syndrome / genetics. Hamartoma / complications. Hamartoma / diagnosis. Point Mutation. Receptors, Androgen / genetics. Testicular Diseases / complications

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  • [ErratumIn] Hormones (Athens). 2006 Oct-Dec;5(4):following 311
  • (PMID = 16950754.001).
  • [ISSN] 1109-3099
  • [Journal-full-title] Hormones (Athens, Greece)
  • [ISO-abbreviation] Hormones (Athens)
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Greece
  • [Chemical-registry-number] 0 / Glycoproteins; 0 / Receptors, Androgen; 0 / Testicular Hormones; 08J2K08A3Y / Dihydrotestosterone; 80497-65-0 / Anti-Mullerian Hormone; 9002-68-0 / Follicle Stimulating Hormone
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34. Hutter J, Reich-Weinberger S, Hutarew G, Stein HJ: Giant pulmonary hamartoma--a rare presentation of a common tumor. Ann Thorac Surg; 2006 Aug;82(2):e5-7
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  • [Title] Giant pulmonary hamartoma--a rare presentation of a common tumor.
  • Hamartomata, the most common benign tumors of the lung, are rarely symptomatic and usually come to clinical attention as coin-shaped lesions on a routine plain chest roentgenogram.
  • The histopathology work-up showed pulmonary hamartoma.
  • [MeSH-major] Hamartoma / pathology. Lung Diseases / pathology

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  • (PMID = 16863731.001).
  • [ISSN] 1552-6259
  • [Journal-full-title] The Annals of thoracic surgery
  • [ISO-abbreviation] Ann. Thorac. Surg.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Netherlands
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35. Ruiz Tovar J, Reguero Callejas ME, Aláez Chillarón AB, Ramiro Pérez C, Collado Guirao MV, Rojo Blanco R, Muñoz Martín-Cámara J, González-Palacios F, García Villanueva A: Mammary hamartoma. Clin Transl Oncol; 2006 Apr;8(4):290-3
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  • [Title] Mammary hamartoma.
  • INTRODUCTION: Mammary hamartomas are rare benign breast lumps.
  • Mammary hamartoma has been classically considered as an underdiagnosed pathology, but with the increasing use of diagnostic procedures in breast tumours, the number of hamartomas has increased in the last years.
  • MATERIALS AND METHODS: The clinicopathological features of 8 mammary hamartomas are reported here.
  • We describe a case of recurrence after excision of the lump in a more aggressive histological form and one patient who presented the coexistence of a mammary hamartoma and an invasive ductal carcinoma.
  • CONCLUSION: Mammary hamartoma is an uncommon breast tumour.
  • [MeSH-major] Breast Diseases / pathology. Hamartoma / pathology

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  • (PMID = 16648106.001).
  • [ISSN] 1699-048X
  • [Journal-full-title] Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico
  • [ISO-abbreviation] Clin Transl Oncol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Spain
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36. Saint-Blancard P, Trueba F: [A rare splenic lesion, the splenoma or splenic hamartoma]. Rev Med Interne; 2009 Jun;30(6):533-6
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  • [Title] [A rare splenic lesion, the splenoma or splenic hamartoma].
  • [Transliterated title] Une lésion rare de la rate, le splénome ou hamartome splénique.
  • Splenoma or splenic hamartoma is a rare primary splenic tumor most often incidentally discovered, radiologically.

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  • (PMID = 18818001.001).
  • [ISSN] 0248-8663
  • [Journal-full-title] La Revue de medecine interne
  • [ISO-abbreviation] Rev Med Interne
  • [Language] FRE
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
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37. Khonsari RH, Lepourry J, Corre P: [Hamartomatous and pluritissular tumors]. Rev Stomatol Chir Maxillofac; 2009 Dec;110(6):340-6
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  • [Title] [Hamartomatous and pluritissular tumors].
  • Hamartoma are defined by the benign proliferation of cells normally occurring in the affected tissue or organ.
  • Hamartoma of the maxilla and mandible are a heterogeneous group of diseases.
  • [MeSH-major] Hamartoma / diagnosis. Jaw Diseases / diagnosis. Jaw Neoplasms / diagnosis

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  • (PMID = 19931105.001).
  • [ISSN] 1776-257X
  • [Journal-full-title] Revue de stomatologie et de chirurgie maxillo-faciale
  • [ISO-abbreviation] Rev Stomatol Chir Maxillofac
  • [Language] fre
  • [Publication-type] English Abstract; Journal Article; Review
  • [Publication-country] France
  • [Number-of-references] 20
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38. Silva VA, Kataguiri P, Trufelli DC, Matos LL, Neves-Pereira JC, Campos JR: [Pulmonary hamartoma as a differential diagnosis of breast cancer metastasis: case report]. J Bras Pneumol; 2007 Nov-Dec;33(6):738-42
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  • [Title] [Pulmonary hamartoma as a differential diagnosis of breast cancer metastasis: case report].
  • [Transliterated title] Hamartoma pulmonar como diagnóstico diferencial de metástase de carcinoma de mama: relato de caso.
  • After thoracoscopic nodulectomy, the frozen section analysis revealed a pulmonary hamartoma.
  • Recent studies show that 75% of patients who undergo surgery for pulmonary nodules after a curative mastectomy for breast cancer present lung metastases, 11.5% present primary lung cancer, and 13.5% present benign lesions, including hamartoma.
  • [MeSH-major] Breast Neoplasms / pathology. Carcinoma / pathology. Hamartoma / pathology. Lung Diseases / pathology

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  • (PMID = 18200376.001).
  • [ISSN] 1806-3756
  • [Journal-full-title] Jornal brasileiro de pneumologia : publicaça̋o oficial da Sociedade Brasileira de Pneumologia e Tisilogia
  • [ISO-abbreviation] J Bras Pneumol
  • [Language] por
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Brazil
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39. Sardinoux M, Raingeard I, Bessis D, Coupier I, Renard E, Bringer J: [Cowden syndrome, or multiple hamartomatous tumor syndrome, in clinical endocrinology]. Ann Endocrinol (Paris); 2010 Sep;71(4):264-73
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  • [Title] [Cowden syndrome, or multiple hamartomatous tumor syndrome, in clinical endocrinology].
  • [Transliterated title] Le syndrome de Cowden ou syndrome des hamartomes multiples en endocrinologie clinique.
  • Cowden syndrome (CS) is the prototypic PTEN hamartoma tumor syndromes (PHTS), rare clinical syndromes characterized by germline mutations of the tumor suppressor PTEN.
  • The association in a patient with thyroid cancer, rarely with multinodular goiter, of typical dermatological manifestations, easily identifiable by clinical examination (papillomatous papules, acral keratoses, trichilemmomas), with a history of breast, endometrial, or renal cancer, or hamartomatous tumors presence, should alert the clinician.
  • [MeSH-major] Antineoplastic Agents / therapeutic use. Hamartoma Syndrome, Multiple / diagnosis. Hamartoma Syndrome, Multiple / drug therapy. PTEN Phosphohydrolase / antagonists & inhibitors

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  • [Copyright] Copyright 2010 Elsevier Masson SAS. All rights reserved.
  • (PMID = 20627233.001).
  • [ISSN] 0003-4266
  • [Journal-full-title] Annales d'endocrinologie
  • [ISO-abbreviation] Ann. Endocrinol. (Paris)
  • [Language] fre
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] France
  • [Chemical-registry-number] 0 / Antineoplastic Agents; EC 2.7.1.- / Phosphatidylinositol 3-Kinases; EC 2.7.1.1 / TOR Serine-Threonine Kinases; EC 2.7.11.1 / Proto-Oncogene Proteins c-akt; EC 3.1.3.67 / PTEN Phosphohydrolase
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40. Company MM, Usamentiaga E, Torralba J, Bonet L: [Small bowel diaphragm disease associated with NSAIDs with histology of neuromuscular and vascular hamartoma. Case report and literature review]. Gastroenterol Hepatol; 2005 Apr;28(4):228-31
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  • [Title] [Small bowel diaphragm disease associated with NSAIDs with histology of neuromuscular and vascular hamartoma. Case report and literature review].
  • [Transliterated title] Enfermedad diafragmática intestinal asociada a AINE con histología de hamartoma neuromuscular y vascular. Presentación de un caso y revisión de la bibliografía.
  • Diaphragm disease (DD) induced by non-steroidal anti-inflammatory drugs (NSAIDs) and neuromuscular and vascular hamartoma (NMVH) are rare entities that can be difficult to recognize clinically, radiologically and pathologically.
  • However, the 2 entities differ in that the constrictions are purely fibrous in DD whereas they have a hamartomatous histopathology in NMVH.
  • [MeSH-major] Anti-Inflammatory Agents, Non-Steroidal / adverse effects. Hamartoma / chemically induced. Ileal Diseases / chemically induced. Intestinal Obstruction / etiology

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  • (PMID = 15811265.001).
  • [ISSN] 0210-5705
  • [Journal-full-title] Gastroenterología y hepatología
  • [ISO-abbreviation] Gastroenterol Hepatol
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article; Review
  • [Publication-country] Spain
  • [Chemical-registry-number] 0 / Anti-Inflammatory Agents, Non-Steroidal
  • [Number-of-references] 14
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41. Benkirane A, Berrebi D, Olaya N, Ferkdadji L, Chomette PP, Benkerrou M, Peuchmaur M: [Hamartoma of the spleen (splenoma) in a child with sickle cell anemia]. Ann Pathol; 2007 Feb;27(1):27-30
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  • [Title] [Hamartoma of the spleen (splenoma) in a child with sickle cell anemia].
  • [Transliterated title] Hamartome de la rate (splénome) chez un enfant drépanocytaire.
  • Hamartomas of the spleen or splenomas are uncommon benign lesions that predominantly occur in adults.
  • We report a case of an 11-year-old girl with sickle cell anemia who had a single splenic 1.8 cm nodule incidentally found during splenectomy and histologically characterized by disorganized red pulp tissue without interspersed white pulp leading to the diagnosis of hamartoma.
  • The association of hamartoma and hematological conditions is a very unusual condition in children.
  • [MeSH-major] Anemia, Sickle Cell / complications. Hamartoma / pathology. Splenic Neoplasms / pathology


42. Kurkcuoglu IC, Demircan S, Kurul IC, Demirag F: Endobronchial lipomatous hamartoma. Asian Cardiovasc Thorac Ann; 2005 Dec;13(4):372-3
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  • [Title] Endobronchial lipomatous hamartoma.
  • Pulmonary hamartomas are the most common benign neoplasm of the lung, occurring in the parenchyma or sometimes within the bronchi.
  • Sleeve left upper lobectomy was performed and histopathological examination revealed multiple growths of endobronchial hamartomatous foci.
  • This report demonstrates that endobronchial hamartomas may develop from multiple foci.
  • [MeSH-major] Bronchial Neoplasms / pathology. Hamartoma Syndrome, Multiple / pathology. Lipomatosis / pathology

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  • (PMID = 16304229.001).
  • [ISSN] 0218-4923
  • [Journal-full-title] Asian cardiovascular & thoracic annals
  • [ISO-abbreviation] Asian Cardiovasc Thorac Ann
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Singapore
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43. Hamdi R, De Korvin H, Speeg-Schatz C, Szwarcberg J: [Combined hamartoma of the retina and retinal pigment epithelium. Four case studies]. J Fr Ophtalmol; 2006 Mar;29(3):e6
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  • [Title] [Combined hamartoma of the retina and retinal pigment epithelium. Four case studies].
  • [Transliterated title] Hamartome combiné de l'épithélium pigmentaire et de la rétine. A propos de 4 cas.
  • INTRODUCTION: Combined hamartoma of the retina and retinal pigment epithelium is a rare condition, characterized by a proliferation of the retinal pigmentary epithelium and retinal gliosis leading to a disorganization of the retina and papilla.
  • OBSERVATIONS: We report a series of four children followed between 2001 and 2004 with combined hamartoma of the retina and retinal pigment epithelium, with age of diagnosis ranging from 3 months to 8 years.
  • DISCUSSION: Combined hamartoma of the retina and retinal pigment epithelium is probably a congenital tumor whose pathogenesis has not yet been elucidated.
  • In this disorder, it is important to eliminate retinoblastoma and malignant melanoma of the choroid, showing the advantage of radiological exploration.
  • [MeSH-major] Hamartoma. Pigment Epithelium of Eye. Retinal Neoplasms

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  • (PMID = 16557165.001).
  • [ISSN] 1773-0597
  • [Journal-full-title] Journal français d'ophtalmologie
  • [ISO-abbreviation] J Fr Ophtalmol
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
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44. Saadat P, Doostan A, Vadmal MS: Folliculosebaceous smooth muscle hamartoma. J Am Acad Dermatol; 2007 Jun;56(6):1021-5
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  • [Title] Folliculosebaceous smooth muscle hamartoma.
  • Cutaneous hamartomas are a group of heterogenous benign skin conditions demonstrating epithelial and mesenchymal components in varying proportions.
  • Folliculosebaceous (cystic) hamartomas comprise a distinct group of uncommon cutaneous tumor-like malformations.
  • We review the literature on folliculosebaceous hamartoma and report a case with smooth muscle as its only stromal component.
  • [MeSH-major] Hamartoma / pathology. Muscle, Smooth / pathology. Muscular Diseases / pathology

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  • (PMID = 17504719.001).
  • [ISSN] 1097-6787
  • [Journal-full-title] Journal of the American Academy of Dermatology
  • [ISO-abbreviation] J. Am. Acad. Dermatol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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45. Pérez-Alvarez MJ, Alejandre-Alba N, García-Sánchez J: [Combined hamartoma of the retina and retinal pigment epithelium diagnosed by retinal angiography and optical coherence tomography]. Arch Soc Esp Oftalmol; 2008 Mar;83(3):193-6
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  • [Title] [Combined hamartoma of the retina and retinal pigment epithelium diagnosed by retinal angiography and optical coherence tomography].
  • [Transliterated title] Hamartoma combinado de retina y epitelio pigmentario retiniano. Diagnóstico mediante tomografía de coherencia óptica y angiofluoresceingrafía.
  • CLINICAL CASE: This report is based on the case of a 35-year-old woman who developed a combined hamartoma of the retina and retinal pigment epithelium in her right eye.
  • [MeSH-major] Hamartoma / pathology. Hamartoma / radiography. Pigment Epithelium of Eye. Retinal Diseases / pathology. Retinal Diseases / radiography. Tomography, Optical Coherence

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  • (PMID = 18311679.001).
  • [ISSN] 0365-6691
  • [Journal-full-title] Archivos de la Sociedad Española de Oftalmología
  • [ISO-abbreviation] Arch Soc Esp Oftalmol
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Spain
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46. Ayadi-Kaddour A, Saïji E, Ben Slama S, Chelly-Ennaiffer I, Lahmar-Boufaroua A, Goutallier-Ben Fadhel C, Ben Sassi L, Khalfallah MT, Mzabi-Regaya S: [Hepatic mesenchymal hamartoma in adulthood: a case report with literature review]. Tunis Med; 2006 Apr;84(4):263-5
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  • [Title] [Hepatic mesenchymal hamartoma in adulthood: a case report with literature review].
  • [Transliterated title] Hamartome mesenchymateux du foie chez l'adulte: a propos d'un cas avec revue de la littérature.
  • Mesenchymal hamartoma is a rare and benign tumor..
  • Authors report a new case of hepatic mesenchymal hamartoma in a 21-year-old woman, diagnosed after a sudden onser of clinical and biological cholestasis.
  • The diagnosis of hepatic mesenchymal hamartoma was based onn hitology of the resected liver specimen.
  • [MeSH-major] Hamartoma / pathology. Liver Diseases / pathology

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  • (PMID = 16833000.001).
  • [ISSN] 0041-4131
  • [Journal-full-title] La Tunisie médicale
  • [ISO-abbreviation] Tunis Med
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article; Review
  • [Publication-country] Tunisia
  • [Number-of-references] 11
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47. Gonul E, Yetiser S, Tasar M, Ongoru O: Glioneural hamartoma of the VIIIth nerve. J Laryngol Otol; 2006 Jan;120(1):70-3
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  • [Title] Glioneural hamartoma of the VIIIth nerve.
  • Hamartomas of the cerebellopontine angle or internal auditory canal are very rare and only four cases have been reported.
  • We report an unusual case of a glioneural hamartoma of the VIIIth nerve with clinical, radiological and audiometric similarity with vestibular schwannoma.
  • [MeSH-major] Hamartoma / diagnosis. Vestibulocochlear Nerve Diseases / diagnosis

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  • (PMID = 16359152.001).
  • [ISSN] 0022-2151
  • [Journal-full-title] The Journal of laryngology and otology
  • [ISO-abbreviation] J Laryngol Otol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
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48. Baba M, Hong SB, Sharma N, Warren MB, Nickerson ML, Iwamatsu A, Esposito D, Gillette WK, Hopkins RF 3rd, Hartley JL, Furihata M, Oishi S, Zhen W, Burke TR Jr, Linehan WM, Schmidt LS, Zbar B: Folliculin encoded by the BHD gene interacts with a binding protein, FNIP1, and AMPK, and is involved in AMPK and mTOR signaling. Proc Natl Acad Sci U S A; 2006 Oct 17;103(42):15552-7
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  • Birt-Hogg-Dubé syndrome, a hamartoma disorder characterized by benign tumors of the hair follicle, lung cysts, and renal neoplasia, is caused by germ-line mutations in the BHD(FLCN) gene, which encodes a tumor-suppressor protein, folliculin (FLCN), with unknown function.
  • The tumor-suppressor proteins encoded by genes responsible for several other hamartoma syndromes, LKB1, TSC1/2, and PTEN, have been shown to be involved in the mammalian target of rapamycin (mTOR) signaling pathway.

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  • [Cites] Biochem J. 2000 Feb 1;345 Pt 3:437-43 [10642499.001]
  • [Cites] Dev Biol. 2006 Mar 15;291(2):227-38 [16443210.001]
  • [Cites] Oncogene. 2001 Aug 23;20(37):5239-42 [11526515.001]
  • [Cites] Am J Hum Genet. 2001 Oct;69(4):876-82 [11533913.001]
  • [Cites] Bioessays. 2001 Dec;23(12):1112-9 [11746230.001]
  • [Cites] Cancer Epidemiol Biomarkers Prev. 2002 Apr;11(4):393-400 [11927500.001]
  • [Cites] Cancer Cell. 2002 Aug;2(2):157-64 [12204536.001]
  • [Cites] Nat Cell Biol. 2002 Sep;4(9):648-57 [12172553.001]
  • [Cites] Nat Cell Biol. 2002 Sep;4(9):658-65 [12172554.001]
  • [Cites] Am J Surg Pathol. 2002 Dec;26(12):1542-52 [12459621.001]
  • [Cites] J Med Genet. 2002 Dec;39(12):906-12 [12471204.001]
  • [Cites] Oncogene. 2003 May 8;22(18):2728-38 [12743597.001]
  • [Cites] Genes Dev. 2003 Aug 1;17(15):1829-34 [12869586.001]
  • [Cites] Hum Mutat. 2003 Sep;22(3):183-98 [12938083.001]
  • [Cites] Curr Biol. 2003 Nov 11;13(22):2004-8 [14614828.001]
  • [Cites] Cell. 2003 Nov 26;115(5):577-90 [14651849.001]
  • [Cites] Sci STKE. 2003 Dec 9;2003(212):re15 [14668532.001]
  • [Cites] Trends Biochem Sci. 2004 Jan;29(1):18-24 [14729328.001]
  • [Cites] Proc Natl Acad Sci U S A. 2004 Mar 9;101(10):3329-35 [14985505.001]
  • [Cites] Oncogene. 2004 Apr 19;23(18):3151-71 [15094765.001]
  • [Cites] Genes Dev. 2004 Jul 1;18(13):1533-8 [15231735.001]
  • [Cites] Cancer Cell. 2004 Jul;6(1):7-10 [15261137.001]
  • [Cites] Cancer Cell. 2004 Jul;6(1):91-9 [15261145.001]
  • [Cites] Mod Pathol. 2004 Aug;17(8):998-1011 [15143337.001]
  • [Cites] J Cell Sci. 2004 Nov 1;117(Pt 23):5479-87 [15509864.001]
  • [Cites] Arch Dermatol. 1977 Dec;113(12):1674-7 [596896.001]
  • [Cites] Eur J Biochem. 1989 Dec 8;186(1-2):123-8 [2574667.001]
  • [Cites] Electrophoresis. 1992 Mar;13(3):142-7 [1592044.001]
  • [Cites] Rapid Commun Mass Spectrom. 1996;10(11):1371-8 [8805846.001]
  • [Cites] Nat Genet. 1998 Jan;18(1):38-43 [9425897.001]
  • [Cites] Nature. 1998 Jan 8;391(6663):184-7 [9428765.001]
  • [Cites] Proc Natl Acad Sci U S A. 1999 Apr 13;96(8):4240-5 [10200246.001]
  • [Cites] Curr Opin Cell Biol. 1999 Apr;11(2):219-25 [10209156.001]
  • [Cites] Arch Dermatol. 1999 Oct;135(10):1195-202 [10522666.001]
  • [Cites] Curr Mol Med. 2004 Dec;4(8):813-24 [15579028.001]
  • [Cites] Nat Genet. 2005 Jan;37(1):19-24 [15624019.001]
  • [Cites] Curr Opin Cell Biol. 2005 Apr;17(2):158-66 [15780592.001]
  • [Cites] Am J Hum Genet. 2005 Jun;76(6):1023-33 [15852235.001]
  • [Cites] J Natl Cancer Inst. 2005 Jun 15;97(12):931-5 [15956655.001]
  • [Cites] Curr Opin Cell Biol. 2005 Dec;17(6):596-603 [16226444.001]
  • [Cites] Hum Genet. 2000 Aug;107(2):97-114 [11030407.001]
  • (PMID = 17028174.001).
  • [ISSN] 0027-8424
  • [Journal-full-title] Proceedings of the National Academy of Sciences of the United States of America
  • [ISO-abbreviation] Proc. Natl. Acad. Sci. U.S.A.
  • [Language] ENG
  • [Databank-accession-numbers] GENBANK/ DQ145719
  • [Grant] United States / NCI NIH HHS / CO / N01-CO-12400; United States / Intramural NIH HHS / /
  • [Publication-type] Journal Article; Research Support, N.I.H., Extramural; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Carrier Proteins; 0 / FLCN protein, human; 0 / FNIP1 protein, human; 0 / Multienzyme Complexes; 0 / Multiprotein Complexes; 0 / Proteins; 0 / Proto-Oncogene Proteins; 0 / Tumor Suppressor Proteins; EC 2.7.- / Protein Kinases; EC 2.7.1.1 / MTOR protein, human; EC 2.7.1.1 / TOR Serine-Threonine Kinases; EC 2.7.11.1 / AMP-Activated Protein Kinases; EC 2.7.11.1 / Protein-Serine-Threonine Kinases
  • [Other-IDs] NLM/ PMC1592464
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49. Ganti S, Milton R, Davidson L, Anikin V: Giant pulmonary hamartoma. J Cardiothorac Surg; 2006;1:19
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  • [Title] Giant pulmonary hamartoma.
  • Pulmonary hamartomas are usually an incidental finding and range in size from 1 cm to 8 cm in diameter in various series.
  • We report a case of a massive pulmonary hamartoma (size 25.5 x 17.5 x 6.5 cm and weighing 1134 g) in a 61 year old male who presented with a short history of breathlessness.
  • It was successfully treated by surgical resection and final histology was pulmonary hamartoma with predominantly adipose and leiomyomatous differentiation.
  • [MeSH-major] Hamartoma. Lung Neoplasms

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  • [Cites] Thorax. 1987 Oct;42(10):790-3 [3321538.001]
  • [Cites] Chest. 2002 Jul;122(1):202-5 [12114359.001]
  • [Cites] Chest. 1976 Sep;70(03):332-6 [954458.001]
  • [Cites] Mayo Clin Proc. 1996 Jan;71(1):14-20 [8538225.001]
  • [Cites] J Thorac Cardiovasc Surg. 1994 Feb;107(2):611-4 [8302082.001]
  • [Cites] Eur J Cardiothorac Surg. 1990;4(1):15-8 [2407277.001]
  • (PMID = 16887035.001).
  • [ISSN] 1749-8090
  • [Journal-full-title] Journal of cardiothoracic surgery
  • [ISO-abbreviation] J Cardiothorac Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
  • [Other-IDs] NLM/ PMC1552053
  • [General-notes] NLM/ Original DateCompleted: 20070719
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50. Okubo T, Shimazaki T, Shindo G, Kitashiro N, Tsukamoto T: [Non-chondromatous hamartoma]. Kyobu Geka; 2008 Nov;61(12):1053-6
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  • [Title] [Non-chondromatous hamartoma].
  • Pathological examination revealed non-chondromatous hamartoma of the lung.
  • Non-chondromatous hamartoma should be considered in the differential diagnosis of pulmonary nodles.
  • We report a rare case of non-chondromatous hamartoma.
  • [MeSH-major] Hamartoma / pathology. Lung Diseases / pathology

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  • (PMID = 19048907.001).
  • [ISSN] 0021-5252
  • [Journal-full-title] Kyobu geka. The Japanese journal of thoracic surgery
  • [ISO-abbreviation] Kyobu Geka
  • [Language] jpn
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Japan
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51. Romanelli P, Muacevic A, Striano S: Radiosurgery for hypothalamic hamartomas. Neurosurg Focus; 2008;24(5):E9
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  • [Title] Radiosurgery for hypothalamic hamartomas.
  • Radiosurgery plays an important role in the treatment of refractory seizures induced by hypothalamic hamartomas (HHs).
  • [MeSH-major] Cranial Irradiation / methods. Hamartoma / surgery. Hypothalamic Diseases / surgery. Radiosurgery

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  • (PMID = 18447748.001).
  • [ISSN] 1092-0684
  • [Journal-full-title] Neurosurgical focus
  • [ISO-abbreviation] Neurosurg Focus
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 54
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52. Yancovitz M, Gonzalez ME, Votava HJ, Walters R, Kundu R, Shupack JL: Acquired smooth-muscle hamartoma. Dermatol Online J; 2009;15(8):12
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  • [Title] Acquired smooth-muscle hamartoma.
  • Histopathologic examination showed changes that were consistent with a smooth-muscle hamartoma.
  • Cutaneous smooth-muscle hamartomas are uncommon benign neoplasms.
  • [MeSH-major] Hamartoma / pathology. Skin Diseases / pathology

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  • (PMID = 19891920.001).
  • [ISSN] 1087-2108
  • [Journal-full-title] Dermatology online journal
  • [ISO-abbreviation] Dermatol. Online J.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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53. Flann S, Munn SE: Precalcaneal congenital fibrolipomatous hamartoma. Clin Exp Dermatol; 2009 Jun;34(4):495-6
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  • [Title] Precalcaneal congenital fibrolipomatous hamartoma.
  • Precalcaneal congenital fibrolipomatous hamartoma (PCFH) is a condition that is seldom reported in the paediatric literature and rarely in the dermatological literature.
  • We describe this disorder in the male twin of a pair of nonidentical twins.
  • [MeSH-major] Diseases in Twins / congenital. Foot Dermatoses / congenital. Hamartoma / congenital

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  • (PMID = 19183410.001).
  • [ISSN] 1365-2230
  • [Journal-full-title] Clinical and experimental dermatology
  • [ISO-abbreviation] Clin. Exp. Dermatol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
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54. Gholoum S, Fraser R, Ferri LE: Posterior mediastinal chondromatous hamartoma. Ann Thorac Surg; 2007 Apr;83(4):1528-30
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  • [Title] Posterior mediastinal chondromatous hamartoma.
  • Pathologic examination showed it to be a chondromatous hamartoma, representing a very unusual location for this type of tumor.
  • [MeSH-major] Aortic Aneurysm, Thoracic / diagnosis. Hamartoma / diagnosis. Mediastinal Diseases / diagnosis. Thoracic Surgery, Video-Assisted / methods

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  • (PMID = 17383376.001).
  • [ISSN] 1552-6259
  • [Journal-full-title] The Annals of thoracic surgery
  • [ISO-abbreviation] Ann. Thorac. Surg.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Netherlands
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55. Vázquez-Lima I, Vázquez JL, Gallego M, Fernández R, Fernández P: Torsed pedunculated hepatic hamartoma. Pediatr Radiol; 2009 Jan;39(1):62-5
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  • [Title] Torsed pedunculated hepatic hamartoma.
  • We report a 9-year-old boy with a 6-h history of acute abdominal pain due to torsion of a pedunculated hepatic mesenchymal hamartoma.
  • Mesenchymal hepatic hamartomas are unusual tumours that may be pedunculated, and this is a unique case complicated by torsion.
  • [MeSH-major] Hamartoma / radiography. Hamartoma / ultrasonography. Liver Diseases / radiography. Liver Diseases / ultrasonography. Torsion Abnormality / radiography. Torsion Abnormality / ultrasonography

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  • (PMID = 18795278.001).
  • [ISSN] 0301-0449
  • [Journal-full-title] Pediatric radiology
  • [ISO-abbreviation] Pediatr Radiol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Contrast Media
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56. Nagata S, Yamaguchi K, Inoue T, Yamaguchi H, Ito T, Gibo J, Tanaka M, Tsuneyoshi M: Solid pancreatic hamartoma. Pathol Int; 2007 May;57(5):276-80
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  • [Title] Solid pancreatic hamartoma.
  • A case of solid pancreatic hamartoma in a 58-year-old Japanese woman is presented.
  • The histological diagnosis was solid hamartoma of the pancreas.
  • Herein is reported a case of solid hamartoma of the pancreas and review of the literature.
  • A search through the literature found only two cases of solid hamartoma of the pancreas, among the 14 cases previously reported as pancreatic hamartoma.
  • [MeSH-major] Hamartoma / pathology. Pancreatic Diseases / pathology

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  • (PMID = 17493175.001).
  • [ISSN] 1320-5463
  • [Journal-full-title] Pathology international
  • [ISO-abbreviation] Pathol. Int.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Australia
  • [Chemical-registry-number] 0 / Antigens, CD34; EC 2.7.10.1 / Proto-Oncogene Proteins c-kit
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57. Seda G, Amundson D, Lin MY: Predominant cartilaginous hamartoma: an unusual variant of chondromatous hamartoma. South Med J; 2010 Feb;103(2):169-71
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Predominant cartilaginous hamartoma: an unusual variant of chondromatous hamartoma.
  • Chondromatous hamartomas are the most common benign lung tumors and the third most common pulmonary nodule.
  • We report the case of a healthy, 60-year-old woman with an incidentally discovered chondromatous hamartoma that was thorascopically excised.
  • Her pulmonary hamartoma was predominantly cartilaginous, which only occurs in 1% of hamartomas.
  • [MeSH-major] Hamartoma / diagnosis. Lung Diseases / diagnosis

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  • (PMID = 20065908.001).
  • [ISSN] 1541-8243
  • [Journal-full-title] Southern medical journal
  • [ISO-abbreviation] South. Med. J.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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58. Calva D, Howe JR: Hamartomatous polyposis syndromes. Surg Clin North Am; 2008 Aug;88(4):779-817, vii
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  • [Title] Hamartomatous polyposis syndromes.
  • Since the histologic description of the hamartomatous polyp in 1957 by Horrilleno and colleagues, descriptions have appeared of several different syndromes with the propensity to develop these polyps in the upper and lower gastrointestinal tracts.
  • These syndromes include juvenile polyposis, Peutz-Jeghers syndrome, hereditary mixed polyposis syndrome, and the phosphatase and tensin homolog gene (PTEN) hamartoma tumor syndromes (Cowden and Bannayan-Riley-Ruvalcaba syndromes), which are autosomal-dominantly inherited, and Cronkhite-Canada syndrome, which is acquired.
  • This article reviews the clinical aspects, the molecular pathogenesis, the affected organ systems, the risks of cancer, and the management of these hamartomatous polyposis syndromes.

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  • [Cites] Science. 1998 May 15;280(5366):1036-7 [9616081.001]
  • [Cites] Hum Mol Genet. 1998 Nov;7(12):1907-12 [9811934.001]
  • [Cites] J Med Genet. 1998 Nov;35(11):886-9 [9832032.001]
  • [Cites] Ann Surg Oncol. 1998 Dec;5(8):751-6 [9869523.001]
  • [Cites] Curr Probl Surg. 2005 May;42(5):267-333 [15900295.001]
  • [Cites] Zhonghua Wei Chang Wai Ke Za Zhi. 2005 Jul;8(4):312-5 [16167249.001]
  • [Cites] J Mol Diagn. 2006 Feb;8(1):84-8 [16436638.001]
  • [Cites] J Med Genet. 2006 Mar;43(3):e13 [16525031.001]
  • [Cites] Clin Gastroenterol Hepatol. 2006 Apr;4(4):408-15 [16616343.001]
  • [Cites] J Med Genet. 2006 May;43(5):e18 [16648371.001]
  • [Cites] Am J Hum Genet. 2006 Jul;79(1):23-30 [16773562.001]
  • [Cites] Gut. 2007 Jul;56(7):965-7 [17303595.001]
  • [Cites] Am J Surg Pathol. 2007 Aug;31(8):1209-14 [17667545.001]
  • [Cites] N Engl J Med. 2007 Aug 23;357(8):e9 [17715405.001]
  • [Cites] Z Gastroenterol. 2007 Oct;45(10):1049-55 [17924301.001]
  • [Cites] J Med Genet. 2007 Nov;44(11):702-9 [17873119.001]
  • [Cites] Clin Exp Dermatol. 2008 Mar;33(2):151-3 [18021272.001]
  • [Cites] N Engl J Med. 1949 Dec 22;241(25):993, illust; passim [15399020.001]
  • [Cites] JAMA. 1970 Jan 5;211(1):120-2 [5466889.001]
  • [Cites] Ann Surg Oncol. 1995 Sep;2(5):386-91 [7496832.001]
  • [Cites] Gastroenterology. 1970 May;58(5):699-708 [5444174.001]
  • [Cites] Cancer. 1970 May;25(5):1107-21 [5429475.001]
  • [Cites] Cancer. 1970 Dec;26(6):1232-8 [5483654.001]
  • [Cites] Arch Pathol. 1971 Jul;92(1):1-5 [5091590.001]
  • [Cites] Dis Colon Rectum. 1971 Sep-Oct;14(5):368-74 [5096013.001]
  • [Cites] J Ky Med Assoc. 1972 Jul;70(7):540-4 [5038441.001]
  • [Cites] J Surg Oncol. 1972;4(4):354-62 [5083569.001]
  • [Cites] Surgery. 1974 Jan;75(1):107-14 [4543470.001]
  • [Cites] Ann Intern Med. 1975 Nov;83(5):639-46 [1200496.001]
  • [Cites] JAMA. 1977 Jul 4;238(1):26 [577252.001]
  • [Cites] South Med J. 1977 Jul;70(7):882-4 [877657.001]
  • [Cites] Gastroenterology. 1978 Jun;74(6):1325-30 [348556.001]
  • [Cites] Cancer. 1979 May;43(5):1906-13 [445378.001]
  • [Cites] Gastroenterology. 1979 Jul;77(1):148-51 [447014.001]
  • [Cites] Br J Dermatol. 1979 Jun;100(6):667-73 [465314.001]
  • [Cites] Gastroenterology. 1979 Dec;77(6):1311-5 [499717.001]
  • [Cites] Cancer. 1980 Jul 1;46(1):223-8 [6770991.001]
  • [Cites] Postgrad Med J. 1980 May;56(655):373-6 [7003570.001]
  • [Cites] Clin Genet. 1980 Dec;18(6):413-6 [7449178.001]
  • [Cites] Histopathology. 1981 Jul;5(4):361-76 [7275020.001]
  • [Cites] Cancer. 1982 Apr 1;49(7):1500-3 [7059958.001]
  • [Cites] Pediatrics. 1982 May;69(5):632-4 [7079022.001]
  • [Cites] Cancer. 1982 Oct 1;50(7):1384-402 [7104978.001]
  • [Cites] Medicine (Baltimore). 1982 Sep;61(5):293-309 [7109958.001]
  • [Cites] Gastroenterology. 1988 Dec;95(6):1535-40 [3181678.001]
  • [Cites] Histopathology. 1988 Dec;13(6):619-30 [2853131.001]
  • [Cites] Am J Med Genet. 1989 Jan;32(1):1-8 [2705469.001]
  • [Cites] Am J Surg Pathol. 1989 Nov;13(11):940-6 [2552848.001]
  • [Cites] Am J Gastroenterol. 1989 Nov;84(11):1456-9 [2683746.001]
  • [Cites] Jpn J Surg. 1991 Mar;21(2):220-3 [2051670.001]
  • [Cites] Arch Dis Child. 1991 Aug;66(8):971-5 [1656892.001]
  • [Cites] Cancer. 1992 Jun 15;69(12):2969-74 [1350505.001]
  • [Cites] Cancer. 1992 Aug 15;70(4):869-76 [1643619.001]
  • [Cites] Am J Med Genet. 1992 Oct 1;44(3):307-14 [1336932.001]
  • [Cites] Gastroenterology. 1993 Mar;104(3):910-5 [8440442.001]
  • [Cites] Z Gastroenterol. 1993 Sep;31(9):480-3 [8237087.001]
  • [Cites] Clin Genet. 1993 Dec;44(6):281-6 [8131297.001]
  • [Cites] Am J Clin Pathol. 1994 Jul;102(1):91-7 [8037173.001]
  • [Cites] J Med Genet. 1994 Jun;31(6):458-61 [8071972.001]
  • [Cites] Am J Surg Pathol. 1995 Jan;19(1):50-8 [7802138.001]
  • [Cites] J Pediatr Surg. 1994 Dec;29(12):1584-7 [7877037.001]
  • [Cites] Br J Surg. 1995 Jan;82(1):14-7 [7881943.001]
  • [Cites] J Med Genet. 1995 Feb;32(2):117-9 [7760320.001]
  • [Cites] Nihon Geka Hokan. 1995 Jan 1;64(1):3-14 [8534187.001]
  • [Cites] J Am Coll Surg. 1995 Nov;181(5):407-13 [7582207.001]
  • [Cites] Am J Hum Genet. 1996 Apr;58(4):770-6 [8644741.001]
  • [Cites] Nat Genet. 1996 May;13(1):114-6 [8673088.001]
  • [Cites] Cell. 1996 Jun 28;85(7):947-50 [8674122.001]
  • [Cites] Nat Genet. 1997 Jan;15(1):87-90 [8988175.001]
  • [Cites] Gastroenterology. 1997 Feb;112(2):327-34 [9024286.001]
  • [Cites] Science. 1997 Mar 28;275(5308):1943-7 [9072974.001]
  • [Cites] Nat Genet. 1997 May;16(1):64-7 [9140396.001]
  • [Cites] Nat Genet. 1997 Aug;16(4):333-4 [9241266.001]
  • [Cites] Hum Mol Genet. 1997 Aug;6(8):1383-7 [9259288.001]
  • [Cites] Am J Med Genet. 1997 Sep 5;71(4):489-93 [9286463.001]
  • [Cites] Gastroenterology. 1997 Nov;113(5):1433-7 [9352843.001]
  • [Cites] Nature. 1997 Dec 4;390(6659):465-71 [9393997.001]
  • [Cites] Nat Genet. 1998 Jan;18(1):38-43 [9425897.001]
  • [Cites] Nature. 1998 Jan 8;391(6663):184-7 [9428765.001]
  • [Cites] Hum Mol Genet. 1998 Mar;7(3):507-15 [9467011.001]
  • [Cites] Am J Hum Genet. 1997 Dec;61(6):1254-60 [9399897.001]
  • [Cites] Am J Hum Genet. 1997 Dec;61(6):1327-34 [9399902.001]
  • [Cites] Am J Hum Genet. 1998 May;62(5):1129-36 [9545410.001]
  • [Cites] Science. 1998 May 15;280(5366):1086-8 [9582123.001]
  • [Cites] Cancer Res. 2000 Jan 1;60(1):70-3 [10646855.001]
  • [Cites] Am J Gastroenterol. 2000 Mar;95(3):596-604 [10710046.001]
  • [Cites] J Gastroenterol. 2000;35(9):706-11 [11023043.001]
  • [Cites] J Med Genet. 2000 Nov;37(11):828-30 [11073535.001]
  • [Cites] Cancer. 1982 Nov 15;50(10):2139-46 [7127254.001]
  • [Cites] J R Soc Med. 1983 Aug;76(8):701-3 [6887190.001]
  • [Cites] J Pediatr. 1983 Oct;103(4):593-5 [6620020.001]
  • [Cites] West J Med. 1983 Sep;139(3):324-8 [6636746.001]
  • [Cites] Dig Dis Sci. 1984 Feb;29(2):178-82 [6321116.001]
  • [Cites] Dis Colon Rectum. 1984 Jun;27(6):393-8 [6734363.001]
  • [Cites] Gut. 1984 Jul;25(7):792-800 [6735258.001]
  • [Cites] Gut. 1984 Oct;25(10):1118-23 [6479688.001]
  • [Cites] Am J Surg Pathol. 1984 Oct;8(10):763-70 [6496844.001]
  • [Cites] Surgery. 1986 Jan;99(1):82-6 [3001960.001]
  • [Cites] Hum Pathol. 1986 Jan;17(1):97-9 [3943856.001]
  • [Cites] Cancer. 1986 Jun 1;57(11):2238-40 [3697923.001]
  • [Cites] Clin Genet. 1986 Mar;29(3):222-33 [3698331.001]
  • [Cites] Arch Surg. 1986 May;121(5):530-4 [3707330.001]
  • [Cites] Am J Hum Genet. 1986 Jun;38(6):908-17 [3487976.001]
  • [Cites] Arch Pathol Lab Med. 1987 Feb;111(2):200-1 [3813837.001]
  • [Cites] Dig Dis Sci. 1987 Aug;32(8):943-6 [3608737.001]
  • [Cites] Int J Colorectal Dis. 1987 Jun;2(2):96-9 [3040875.001]
  • [Cites] Dis Colon Rectum. 1987 Oct;30(10):790-9 [3308369.001]
  • [Cites] Endoscopy. 1988 Jan;20(1):33-5 [2830104.001]
  • [Cites] Gastroenterology. 1999 Apr;116(4):789-95 [10092300.001]
  • [Cites] J Med Genet. 1999 May;36(5):360-4 [10353779.001]
  • [Cites] Genes Chromosomes Cancer. 1999 Aug;25(4):403-6 [10398437.001]
  • [Cites] Hum Mol Genet. 1999 Aug;8(8):1461-72 [10400993.001]
  • [Cites] Genes Chromosomes Cancer. 1999 Sep;26(1):54-61 [10441006.001]
  • [Cites] Surgery. 1999 Aug;126(2):162-70 [10455879.001]
  • [Cites] Scand J Gastroenterol Suppl. 1999;230:64-70 [10499464.001]
  • [Cites] Proc Staff Meet Mayo Clin. 1954 Mar 24;29(6):168-71 [13145642.001]
  • [Cites] N Engl J Med. 1955 Jun 16;252(24):1011-5 [14383952.001]
  • [Cites] N Engl J Med. 1957 Jun 13;256(24):1141-6; contd [13452009.001]
  • [Cites] Cancer. 1957 Nov-Dec;10(6):1210-20 [13489673.001]
  • [Cites] Surg Gynecol Obstet. 1962 Jul;115:1-11 [13865437.001]
  • [Cites] Ann Intern Med. 1963 Jan;58:136-42 [13931122.001]
  • [Cites] Am J Dig Dis. 1963 Nov;8:953-61 [14083822.001]
  • [Cites] JAMA. 1964 Dec 7;190:935-8 [14214503.001]
  • [Cites] Proc R Soc Med. 1964 Oct;57:896-7 [14214792.001]
  • [Cites] Lahey Clin Bull. 1955 Oct;9(6):174-9 [13272311.001]
  • [Cites] Endoscopy. 2004 Dec;36(12):1060-6 [15578295.001]
  • [Cites] J Clin Pathol. 2005 Jan;58(1):15-9 [15623475.001]
  • [Cites] Dig Dis Sci. 2004 Nov-Dec;49(11-12):1906-11 [15628724.001]
  • [Cites] Gastroenterology. 2000 Dec;119(6):1447-53 [11113065.001]
  • [Cites] Exp Cell Res. 2001 Mar 10;264(1):29-41 [11237521.001]
  • [Cites] J Med Genet. 2001 Mar;38(3):159-64 [11238682.001]
  • [Cites] Nat Genet. 2001 Jun;28(2):184-7 [11381269.001]
  • [Cites] Am J Hum Genet. 2001 Oct;69(4):704-11 [11536076.001]
  • [Cites] Hum Genet. 2002 Jul;111(1):108-11 [12136244.001]
  • [Cites] Ann Surg Oncol. 2002 Nov;9(9):901-6 [12417513.001]
  • [Cites] Clin Genet. 2003 Feb;63(2):126-30 [12630959.001]
  • [Cites] Am J Hum Genet. 2003 May;72(5):1261-7 [12696020.001]
  • [Cites] Am J Hum Genet. 2003 Aug;73(2):404-11 [12844284.001]
  • [Cites] J Gastroenterol. 2003;38(8):791-5 [14505136.001]
  • [Cites] Am J Gastroenterol. 2003 Oct;98(10):2317-20 [14572586.001]
  • [Cites] Digestion. 2004;69(1):57-62 [14755154.001]
  • [Cites] J Med Genet. 2004 Jul;41(7):484-91 [15235019.001]
  • [Cites] J Clin Oncol. 2004 Jul 15;22(14):2954-63 [15254063.001]
  • [Cites] Biochem J. 2004 Aug 15;382(Pt 1):1-11 [15193142.001]
  • [Cites] Gastroenterology. 1966 Jan;50(1):107-18 [5900949.001]
  • [Cites] J Med Genet. 1966 Mar;3(1):5-16 [5911834.001]
  • [Cites] Ann Surg. 1967 Jan;165(1):145-51 [6018292.001]
  • [Cites] Am J Surg. 1967 Dec;114(6):839-43 [6060760.001]
  • (PMID = 18672141.001).
  • [ISSN] 0039-6109
  • [Journal-full-title] The Surgical clinics of North America
  • [ISO-abbreviation] Surg. Clin. North Am.
  • [Language] ENG
  • [Grant] United States / NCI NIH HHS / CA / CA098193-01A1; United States / NCI NIH HHS / CA / R01 CA098193; United States / NCI NIH HHS / CA / R01 CA098193-01A1
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 156
  • [Other-IDs] NLM/ NIHMS67434; NLM/ PMC2659506
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59. Ahrens T, Wreesmann P: [Deterioration of vision in conjunction with retinal changes]. Ophthalmologe; 2009 Jun;106(6):554-6
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  • [Transliterated title] Sehverschlecherung bei seltener Netzhautveränderung. Diagnose: Kombiniertes Hamartom der Netzhaut und des retinalen Pigmentepithels.
  • A combined hamartoma of the retinal pigment epithelium and the retina is a rare alteration of the ocular fundus.
  • [MeSH-major] Hamartoma / complications. Hamartoma / diagnosis. Neurocutaneous Syndromes / complications. Neurocutaneous Syndromes / diagnosis. Retinal Diseases / complications. Retinal Diseases / diagnosis. Vision Disorders / diagnosis. Vision Disorders / etiology

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  • (PMID = 19018539.001).
  • [ISSN] 1433-0423
  • [Journal-full-title] Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft
  • [ISO-abbreviation] Ophthalmologe
  • [Language] ger
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Germany
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60. García-Morales I, Marinas A, del Barrio A, Alvarez-Linera J, Herranz JL, Smeyers P, Gil-Nagel A: [Hypothalamic hamartoma: clinical characteristics. Electroencephalogram and brain magnetic resonance imaging in 10 patients]. Neurologia; 2007 Jan-Feb;22(1):11-8
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  • [Title] [Hypothalamic hamartoma: clinical characteristics. Electroencephalogram and brain magnetic resonance imaging in 10 patients].
  • [Transliterated title] Hamartomas hipotalámicos: características clínicas, electroencefalograma y resonancia magnética cerebral en 10 pacientes.
  • INTRODUCTION: We describe clinical findings and electroencephalogram (EEG) in patients with hypothalamic hamartoma and epilepsy.
  • METHODS: Our group includes 10 patients (eight males) with mean age of 17.8 years (range: 7-39) and hypothalamic hamartoma in the brain magnetic resonance imaging (MRI).
  • MRI showed a hypothalamic lesion suggesting hamartoma associated to a dysplastic lesion in one case.
  • CONCLUSIONS: In our group gelastic seizures were an early and constant finding except in one patient.
  • Video-EEG monitoring allows us to identify interictal and ictal patterns that have been described in hypothalamic hamartomas.
  • [MeSH-major] Electroencephalography. Hamartoma / diagnosis. Hamartoma / physiopathology. Hypothalamic Diseases / diagnosis. Hypothalamic Diseases / physiopathology. Magnetic Resonance Imaging

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  • (PMID = 17315098.001).
  • [ISSN] 0213-4853
  • [Journal-full-title] Neurología (Barcelona, Spain)
  • [ISO-abbreviation] Neurologia
  • [Language] spa
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Spain
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61. Otero D, Israel MS, Antero S, Lourenço S: Bilateral adenomatoid odontogenic hamartoma. Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2009 Apr;107(4):e24-6
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  • [Title] Bilateral adenomatoid odontogenic hamartoma.
  • We report the first case of bilateral odontogenic lesions consistent with several cases of unifocal adenomatoid odontogenic hamartoma in the literature.
  • [MeSH-major] Hamartoma / pathology. Mandibular Diseases / pathology

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  • (PMID = 19327632.001).
  • [ISSN] 1528-395X
  • [Journal-full-title] Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics
  • [ISO-abbreviation] Oral Surg Oral Med Oral Pathol Oral Radiol Endod
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
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62. Murat A, Ozdemir H, Yildirim H, Poyraz AK, Ozercan R: Hamartoma of the breast. Australas Radiol; 2007 Oct;51 Spec No.:B37-9
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  • [Title] Hamartoma of the breast.
  • Breast hamartoma is a rare benign tumour that leads to unilateral breast enlargement without a palpable localized mass lesion.
  • Histologically, a hamartoma consists of varying amounts of adipose, gland, fibre and smooth muscle tissue.
  • The characteristic mammographic appearance of hamartoma of breast has distinct mammographic features with circumscription and fat and soft-tissue density surrounded by a thin radiopaque capsule or pseudocapsule.
  • We present histopathological and radiological findings of a 42-year-old female patient with breast hamartoma who has no complaint.
  • [MeSH-major] Breast Neoplasms / diagnosis. Hamartoma / diagnosis. Magnetic Resonance Imaging. Mammography

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  • (PMID = 17875153.001).
  • [ISSN] 0004-8461
  • [Journal-full-title] Australasian radiology
  • [ISO-abbreviation] Australas Radiol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Australia
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63. Tatekawa Y, Kanehiro H, Nakajima Y: Laparoscopic extirpation of splenic hamartoma. Pediatr Surg Int; 2007 Sep;23(9):911-4
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  • [Title] Laparoscopic extirpation of splenic hamartoma.
  • We presented a case of splenic hamartoma.
  • The imaging diagnosis was splenic hamartoma.
  • In pathological findings, the tumor was compatible with hamartoma.
  • Splenic hamartomas in pediatric patients have been described extremely rare.
  • In clinical symptoms, spontaneously ruptured splenic hamartoma has been rarely reported.
  • [MeSH-major] Hamartoma / surgery. Laparoscopy / methods. Splenic Neoplasms / surgery

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  • (PMID = 17364201.001).
  • [ISSN] 0179-0358
  • [Journal-full-title] Pediatric surgery international
  • [ISO-abbreviation] Pediatr. Surg. Int.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Contrast Media; 0 / Lipopolysaccharides; 0 / Polysaccharides; 0 / Re lipopolysaccharide; 127279-08-7 / SHU 508
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64. Athre R, Ducic Y: Frontal sinus hamartomas. Am J Otolaryngol; 2005 Nov-Dec;26(6):419-21
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  • [Title] Frontal sinus hamartomas.
  • OBJECTIVE: To review the entity of respiratory epithelial adenomatoid hamartoma of the paranasal sinuses using an illustrative case example of frontal sinus hamartoma.
  • RESULTS: Respiratory epithelial adenomatoid hamartoma represents a benign process that is generally cured with conservative surgical resection of the involved area.
  • CONCLUSION: Hamartomas of the paranasal sinuses represent a rare entity, which should be considered in the differential diagnosis of expansile sinonasal lesions.
  • [MeSH-major] Frontal Sinus / pathology. Frontal Sinus / surgery. Hamartoma / pathology. Hamartoma / surgery. Paranasal Sinus Diseases / pathology. Paranasal Sinus Diseases / surgery

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  • (PMID = 16275416.001).
  • [ISSN] 0196-0709
  • [Journal-full-title] American journal of otolaryngology
  • [ISO-abbreviation] Am J Otolaryngol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 13
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65. Warren RB, Verbov JL, Ashworth M: Precalcaneal congenital fibrolipomatous hamartoma. Pediatr Dermatol; 2007 Jan-Feb;24(1):74-5
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  • [Title] Precalcaneal congenital fibrolipomatous hamartoma.
  • The diagnosis was precalcaneal congenital fibrolipomatous hamartoma.
  • [MeSH-major] Fibroma / pathology. Hamartoma / congenital. Hamartoma / pathology. Heel / abnormalities. Heel / pathology. Lipoma / pathology. Skin Diseases / congenital. Skin Diseases / pathology

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  • (PMID = 17300657.001).
  • [ISSN] 0736-8046
  • [Journal-full-title] Pediatric dermatology
  • [ISO-abbreviation] Pediatr Dermatol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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66. Kim SK, Kim YC: Neurocristic cutaneous hamartoma of the scalp. Ann Dermatol; 2009 Nov;21(4):396-8
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  • [Title] Neurocristic cutaneous hamartoma of the scalp.
  • Neurocristic cutaneous hamartomas (NCHs) result from aberrant development of the neuromesenchyme.

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  • [Cites] Am J Dermatopathol. 1983 Aug;5(4):385-95 [6314835.001]
  • [Cites] J Dermatol. 1983 Jun;10(3):275-80 [6358316.001]
  • [Cites] Arch Dermatol. 1982 Aug;118(8):592-6 [7103529.001]
  • [Cites] J Am Acad Dermatol. 1996 Apr;34(4):715 [8601674.001]
  • [Cites] Am J Surg Pathol. 1996 Jun;20(6):665-77 [8651345.001]
  • [Cites] Ann Diagn Pathol. 1998 Aug;2(4):213-23 [9845741.001]
  • [Cites] Histopathology. 2006 Sep;49(3):326-8 [16918988.001]
  • [Cites] J Am Acad Dermatol. 1988 Oct;19(4):712-22 [3053804.001]
  • [Cites] J Cutan Pathol. 1993 Oct;20(5):459-64 [8300932.001]
  • [Cites] Mod Pathol. 1998 Jun;11(6):573-8 [9647596.001]
  • [Cites] J Am Acad Dermatol. 2003 Nov;49(5):924-9 [14576682.001]
  • [Cites] J Cutan Pathol. 2007 Aug;34(8):634-9 [17640234.001]
  • (PMID = 20523831.001).
  • [ISSN] 2005-3894
  • [Journal-full-title] Annals of dermatology
  • [ISO-abbreviation] Ann Dermatol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Korea (South)
  • [Other-IDs] NLM/ PMC2861272
  • [Keywords] NOTNLM ; Hamartoma / Neurocristic / Scalp
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67. Jeong E, Park HJ, Oh ST, Lee JY, Cho BK: Late-onset eccrine angiomatous hamartoma on the forehead. Int J Dermatol; 2006 May;45(5):598-9
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  • [Title] Late-onset eccrine angiomatous hamartoma on the forehead.
  • These findings are consistent with eccrine angiomatous hamartoma.
  • [MeSH-major] Hamartoma / diagnosis. Sweat Gland Diseases / diagnosis

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  • (PMID = 16700801.001).
  • [ISSN] 0011-9059
  • [Journal-full-title] International journal of dermatology
  • [ISO-abbreviation] Int. J. Dermatol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 16
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68. Mills O, Thomas LB: Basaloid follicular hamartoma. Arch Pathol Lab Med; 2010 Aug;134(8):1215-9
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  • [Title] Basaloid follicular hamartoma.
  • Basaloid follicular hamartoma is a benign lesion of important consideration because it can be mistaken both clinically and histologically for basal cell carcinoma.
  • The formation of basaloid follicular hamartoma has been linked to a mutation in the patched gene, which is part of the same pathway implicated in nevoid basal cell carcinoma syndrome.
  • While these hamartomas are considered benign lesions, malignant growths have been reported to arise within them, which raises the question, "Is basaloid follicular hamartoma a premalignant lesion?
  • [MeSH-major] Hair Diseases / diagnosis. Hair Follicle / pathology. Hamartoma / diagnosis


69. Jain TP, Srivastava DN, Mittal R, Gamanagatti S: Fibrolipomatous hamartoma of median nerve. Australas Radiol; 2007 Oct;51 Spec No.:B98-B100
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  • [Title] Fibrolipomatous hamartoma of median nerve.
  • Fibrolipomaous hamartoma is a benign neoplasm of nerves, resulting from anomalous growth of fibroadipose tissue of the nerve sheath.
  • [MeSH-major] Fibroma / diagnosis. Hamartoma / diagnosis. Lipoma / diagnosis. Magnetic Resonance Imaging. Median Neuropathy / diagnosis. Peripheral Nervous System Neoplasms / diagnosis

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  • (PMID = 17875173.001).
  • [ISSN] 0004-8461
  • [Journal-full-title] Australasian radiology
  • [ISO-abbreviation] Australas Radiol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Australia
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70. Arita K, Kurisu K, Kiura Y, Iida K, Otsubo H: Hypothalamic hamartoma. Neurol Med Chir (Tokyo); 2005 May;45(5):221-31
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  • [Title] Hypothalamic hamartoma.
  • The incidence of hypothalamic hamartomas (HHs) has increased since the introduction of magnetic resonance (MR) imaging.
  • This review of hypothalamic hamartomas presents current classifications, pathophysiologies, and treatment modalities.
  • [MeSH-major] Hamartoma. Hypothalamic Diseases

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  • (PMID = 15914961.001).
  • [ISSN] 0470-8105
  • [Journal-full-title] Neurologia medico-chirurgica
  • [ISO-abbreviation] Neurol. Med. Chir. (Tokyo)
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] Japan
  • [Number-of-references] 76
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71. Chang HL, Lerwill MF, Goldstein AM: Breast hamartomas in adolescent females. Breast J; 2009 Sep-Oct;15(5):515-20
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  • [Title] Breast hamartomas in adolescent females.
  • Breast hamartomas are uncommon lesions that have not been extensively characterized in the adolescent population.
  • A search of patient records at our institution over a 17-year period identified seven cases of breast hamartomas in patients less than 18 years of age.
  • Breast hamartomas present as painless, palpable masses in the adolescent population.
  • Histologically, the hamartomas consisted of densely packed, enlarged lobules set within a fibrous stroma.
  • Breast hamartomas are rare in the adolescent population.
  • [MeSH-major] Breast Diseases / surgery. Hamartoma / surgery

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  • (PMID = 19624414.001).
  • [ISSN] 1524-4741
  • [Journal-full-title] The breast journal
  • [ISO-abbreviation] Breast J
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 9007-34-5 / Collagen
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72. ul Bari A, Rahman SB: Acquired smooth muscle hamartoma. Indian J Dermatol Venereol Leprol; 2006 Mar-Apr;72(2):178
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  • [Title] Acquired smooth muscle hamartoma.
  • Smooth muscle hamartoma is an uncommon, usually congenital, cutaneous hyperplasia of the arrectores pilorum muscles.
  • The disease started several years ago as multiple small skin-colored papules that subsequently coalesced to form a large soft plaque on the back of the left shoulder.
  • The diagnosis of acquired smooth muscle hamartoma was confirmed on histopathology.
  • [MeSH-major] Hamartoma / pathology. Muscle, Smooth / pathology

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  • (PMID = 16707840.001).
  • [ISSN] 0378-6323
  • [Journal-full-title] Indian journal of dermatology, venereology and leprology
  • [ISO-abbreviation] Indian J Dermatol Venereol Leprol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] India
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73. Dadlani C, Orlow SJ: Eccrine angiomatous hamartoma. Dermatol Online J; 2006;12(5):9
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  • [Title] Eccrine angiomatous hamartoma.
  • The patient was diagnosed with multiple eccrine pilar angiomatous nevi, an unusual variant of eccrine angiomatous hamartomas.
  • The natural course of eccrine angiomatous hamartomas is typically slow growth and benign behavior.
  • [MeSH-major] Eccrine Glands / pathology. Hamartoma / pathology. Skin Neoplasms / pathology

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  • (PMID = 16962024.001).
  • [ISSN] 1087-2108
  • [Journal-full-title] Dermatology online journal
  • [ISO-abbreviation] Dermatol. Online J.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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74. El-Darouti MA, Marzouk SA, Abdel-Halim MR, Zidan AZ, Fawzy MM: Basaloid follicular hamartoma. Int J Dermatol; 2005 May;44(5):361-5
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  • [Title] Basaloid follicular hamartoma.
  • Basaloid follicular hamartoma (BFH) is a unique benign follicular hamartoma characterized by variable clinical presentations, identical histologic features and possible associations with numerous disorders.
  • Basaloid follicular hamartoma may be hereditary or acquired.
  • [MeSH-major] Hair Diseases / pathology. Hair Follicle / pathology. Hamartoma / pathology

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  • (PMID = 15869532.001).
  • [ISSN] 0011-9059
  • [Journal-full-title] International journal of dermatology
  • [ISO-abbreviation] Int. J. Dermatol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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75. Lee PL, Lourduraj LT, Palko MJ 3rd, Jukic DM, English JC 3rd: Hereditary basaloid follicular hamartoma syndrome. Cutis; 2006 Jul;78(1):42-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Hereditary basaloid follicular hamartoma syndrome.
  • Basaloid follicular hamartoma syndrome (BFHS) is a rare adnexal tumor genodermatosis.
  • [MeSH-major] Carcinoma, Basal Cell / diagnosis. Facial Dermatoses / diagnosis. Hamartoma / diagnosis. Hand Dermatoses / diagnosis. Skin Diseases / diagnosis. Skin Neoplasms / diagnosis


76. Taddie KL, Fallat LM: Lipofibromatous hamartoma of nerve. J Foot Ankle Surg; 2007 Mar-Apr;46(2):116-9
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  • [Title] Lipofibromatous hamartoma of nerve.
  • Lipofibromatous hamartoma is an uncommon, benign, fibrofatty tumor that can involve peripheral nerve tissue.
  • [MeSH-major] Hamartoma / pathology. Lipomatosis / pathology. Peripheral Nervous System Diseases / pathology

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  • (PMID = 17331871.001).
  • [ISSN] 1067-2516
  • [Journal-full-title] The Journal of foot and ankle surgery : official publication of the American College of Foot and Ankle Surgeons
  • [ISO-abbreviation] J Foot Ankle Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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77. Meyer P, Soennichsen K, Buchenau W: Autosomal dominant precalcaneal congenital fibrolipomatous hamartoma. Pediatr Dermatol; 2005 Jul-Aug;22(4):355-6
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  • [Title] Autosomal dominant precalcaneal congenital fibrolipomatous hamartoma.
  • Precalcaneal congenital fibrolipomatous hamartoma is a rare minor malformation previously reported only as sporadic.
  • We report this finding in three family members from two generations, suggesting autosomal dominant inheritance.
  • [MeSH-major] Foot Dermatoses / diagnosis. Hamartoma / diagnosis

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  • [CommentIn] Pediatr Dermatol. 2007 May-Jun;24(3):339-40 [17542904.001]
  • (PMID = 16060876.001).
  • [ISSN] 0736-8046
  • [Journal-full-title] Pediatric dermatology
  • [ISO-abbreviation] Pediatr Dermatol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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78. Unal E, Koksal Y, Akcoren Z, Tavl L, Gunel E, Kerimoglu U: Mesenchymal hamartoma of the liver mimicking hepatoblastoma. J Pediatr Hematol Oncol; 2008 Jun;30(6):458-60
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  • [Title] Mesenchymal hamartoma of the liver mimicking hepatoblastoma.
  • Mesenchymal hamartoma of the liver is a cystic benign liver mass occurring in children.
  • We report an extremely rare case of mesenchymal hamartoma in an 11-month-old boy.
  • The pathologic examination of the specimen revealed mesenchymal hamartoma.
  • Mesenchymal hamartoma of the liver with increased serum AFP levels may mimic hepatoblastoma if a cytological examination samples only the hepatocellular component of mesenchymal hamartoma.
  • According to our knowledge, this is the first case of the mesenchymal hamartoma of the liver, which showed reduction in serum levels of AFP and involution of the tumor size by preoperative chemotherapy.
  • [MeSH-major] Diagnostic Errors. Hamartoma / pathology. Hepatoblastoma / pathology. Liver Diseases / pathology. alpha-Fetoproteins / analysis

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  • (PMID = 18525464.001).
  • [ISSN] 1077-4114
  • [Journal-full-title] Journal of pediatric hematology/oncology
  • [ISO-abbreviation] J. Pediatr. Hematol. Oncol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / alpha-Fetoproteins
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79. Takeyama J, Hayashi T, Saito M, Shimanuki Y, Watanabe M, Sasano H, Shirane R: Spinal hamartoma associated with spinal dysraphism. Childs Nerv Syst; 2006 Sep;22(9):1098-102
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  • [Title] Spinal hamartoma associated with spinal dysraphism.
  • We therefore should diagnose them as hamartoma rather than lipoma or teratoma.
  • [MeSH-major] Hamartoma / congenital. Lipoma / congenital. Lumbar Vertebrae. Sacrum. Spinal Cord Neoplasms / congenital. Spinal Dysraphism / diagnosis. Spinal Neoplasms / congenital

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  • (PMID = 16328392.001).
  • [ISSN] 0256-7040
  • [Journal-full-title] Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
  • [ISO-abbreviation] Childs Nerv Syst
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
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80. Galan A, McNiff JM: Eccrine angiomatous hamartoma with features resembling verrucous hemangioma. J Cutan Pathol; 2007 Dec;34 Suppl 1:68-70
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  • [Title] Eccrine angiomatous hamartoma with features resembling verrucous hemangioma.
  • Eccrine angiomatous hamartoma (EAH) is a benign malformation characterized by a proliferation of eccrine glands and capillary vessels in the dermis.
  • The vessels were negative for glucose transporter-1 protein (GLUT-1), supporting the impression of hamartoma over that of hemangioma.
  • The findings are unusual and expand the histological spectrum of this hamartoma.
  • [MeSH-major] Eccrine Glands / pathology. Hamartoma / diagnosis. Hemangioma / diagnosis. Sweat Gland Diseases / diagnosis

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  • [CommentIn] J Cutan Pathol. 2008 Dec;35(12):1163; author reply 1164 [18976407.001]
  • (PMID = 17997743.001).
  • [ISSN] 1600-0560
  • [Journal-full-title] Journal of cutaneous pathology
  • [ISO-abbreviation] J. Cutan. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Denmark
  • [Chemical-registry-number] 0 / Biomarkers
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81. Altaner S, Yoruk Y, Bilgi S, Puyan FO, Doganay L, Kutlu K: Multifocal mesenchymal hamartoma of the chest wall. Respirology; 2006 May;11(3):334-8
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  • [Title] Multifocal mesenchymal hamartoma of the chest wall.
  • Chest wall hamartomas are extremely rare.
  • Frequently mesenchymal hamartomas are presented as a single mass and contain some primitive mesenchymal elements such as chondroid and trabecular bone structures.
  • Bilateral chest wall hamartomas are extremely rare and may be confused with malignancy.
  • [MeSH-major] Hamartoma / diagnosis. Thoracic Diseases / diagnosis. Thoracic Wall

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  • (PMID = 16635095.001).
  • [ISSN] 1323-7799
  • [Journal-full-title] Respirology (Carlton, Vic.)
  • [ISO-abbreviation] Respirology
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Australia
  • [Chemical-registry-number] 0 / Vimentin
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82. Kim SA, Um SW, Song JU, Jeon K, Koh WJ, Suh GY, Jung MP, Kwon OJ, Park JH, Yi CA, Han J, Kim H: Bronchoscopic features and bronchoscopic intervention for endobronchial hamartoma. Respirology; 2010 Jan;15(1):150-4
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  • [Title] Bronchoscopic features and bronchoscopic intervention for endobronchial hamartoma.
  • BACKGROUND AND OBJECTIVE: Bronchoscopic resection of endobronchial hamartomas has been reported to have a favourable outcome.
  • This study describes the bronchoscopic features of endobronchial hamartoma and reports the clinical outcome of bronchoscopic intervention.
  • METHODS: A retrospective analysis was conducted of patients with histologically proven endobronchial hamartomas, diagnosed in the 10-year period 1999-2009 to elucidate the clinical, radiological and bronchoscopic features of hamartoma and to describe the clinical outcomes.
  • RESULTS: Seventeen of the 135 patients with pulmonary hamartomas were diagnosed as having endobronchial hamartomas.
  • Calcification and areas of focal fat in the lesion, the diagnostic CT findings of pulmonary hamartoma, were found in two of 16 (12.5%) patients.
  • Bronchoscopic forceps biopsies were performed in 13 patients, which resulted in five patients (38.5%) being diagnosed with endobronchial hamartoma.
  • CONCLUSIONS: Bronchoscopic intervention appears to be a safe and effective method to resect endobronchial hamartomas.
  • [MeSH-major] Bronchi / surgery. Bronchoscopy / methods. Hamartoma / surgery. Lung Diseases / surgery

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  • (PMID = 19947992.001).
  • [ISSN] 1440-1843
  • [Journal-full-title] Respirology (Carlton, Vic.)
  • [ISO-abbreviation] Respirology
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Australia
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83. Uzaslan E, Ebsen M, Freudenberg N, Nakamura S, Costabel U, Guzman J: Reactive alveolar epithelium in chondroid hamartoma of the lung. Acta Cytol; 2005 Mar-Apr;49(2):154-6
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  • [Title] Reactive alveolar epithelium in chondroid hamartoma of the lung.
  • OBJECTIVE: To determine the morphologic characteristics of the nonciliated epithelium found in chondroid hamartoma of the lung.
  • STUDY DESIGN: The morphologic characteristics and immunohistochemical reaction for surfactant protein A of the nonciliated epithelium in chondroid hamartoma of the lung was studied by immunohistochemistry.
  • RESULTS: In all cases, the nonciliated epithelium in chondroid hamartoma showed the morphologic criteria of hyperplastic alveolar type II cells and a very strong positive surfactant protein A reaction in the cytoplasm when compared with alveolar epithelium of the normal lung.
  • CONCLUSION: These findings may indicate that the nonciliated cells found in chondroid hamartoma of the lung are hyperplastic type II cells.
  • This suggests that the alveolar epithelium found in chondroid hamartoma of the lung is a secondary reaction around the hamartoma and not a primary component of the lesion.
  • [MeSH-major] Cartilage / pathology. Hamartoma / pathology. Lung Diseases / pathology. Pulmonary Alveoli / pathology. Respiratory Mucosa / pathology

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  • [ErratumIn] Acta Cytol. 2005 Sep-Oct;49(5):127A. Guzman, Josune [added]
  • (PMID = 15839619.001).
  • [ISSN] 0001-5547
  • [Journal-full-title] Acta cytologica
  • [ISO-abbreviation] Acta Cytol.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers; 0 / Pulmonary Surfactant-Associated Protein A
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84. Pervatikar SK, Rao R, Dinesh US, Parameswaraiah S: Large mammary hamartoma with focal invasive ductal carcinoma. Indian J Pathol Microbiol; 2009 Apr-Jun;52(2):249-51
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  • [Title] Large mammary hamartoma with focal invasive ductal carcinoma.
  • Mammary hamartomas are uncommon benign lesions rarely associated with malignancy.
  • However, the mastectomy specimen revealed the malignant mass within a larger hamartomatous mass.
  • Mammary hamartomas are benign lesions but, on exceedingly rare occasions, they may be involved by incidental, coexisting carcinoma, as illustrated in this case report.
  • [MeSH-major] Breast Neoplasms / diagnosis. Breast Neoplasms / pathology. Carcinoma, Ductal / complications. Carcinoma, Ductal / diagnosis. Hamartoma / complications. Hamartoma / diagnosis

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  • (PMID = 19332930.001).
  • [ISSN] 0974-5130
  • [Journal-full-title] Indian journal of pathology & microbiology
  • [ISO-abbreviation] Indian J Pathol Microbiol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] India
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85. Gow KW, Lee L, Pruthi S, Patterson K, Healey PJ: Mesenchymal hamartoma of the liver. J Pediatr Surg; 2009 Feb;44(2):468-70
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  • [Title] Mesenchymal hamartoma of the liver.
  • Mesenchymal hamartoma of the liver is the second most common benign liver tumor of childhood.
  • To illustrate the radiological and gross operative features, we present a 9-month-old male infant with a mesenchymal hamartoma with classic features.
  • [MeSH-major] Hamartoma. Liver Diseases

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  • (PMID = 19231560.001).
  • [ISSN] 1531-5037
  • [Journal-full-title] Journal of pediatric surgery
  • [ISO-abbreviation] J. Pediatr. Surg.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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86. Bertocchini A, Falappa P, Accinni A, Devito R, Inserra A: Radiofrequency thermoablation in chest wall mesenchymal hamartoma of an infant. Ann Thorac Surg; 2007 Dec;84(6):2091-3
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  • [Title] Radiofrequency thermoablation in chest wall mesenchymal hamartoma of an infant.
  • We report on an infant presenting with a chondroid hamartoma managed with a combined conservative surgical treatment and radiofrequency thermoablation.
  • [MeSH-major] Catheter Ablation / methods. Hamartoma / surgery. Thoracic Diseases / surgery. Thoracic Wall

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  • (PMID = 18036945.001).
  • [ISSN] 1552-6259
  • [Journal-full-title] The Annals of thoracic surgery
  • [ISO-abbreviation] Ann. Thorac. Surg.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Netherlands
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87. Fenoglio KA, Wu J, Kim DY, Simeone TA, Coons SW, Rekate H, Rho JM, Kerrigan JF: Hypothalamic hamartoma: basic mechanisms of intrinsic epileptogenesis. Semin Pediatr Neurol; 2007 Jun;14(2):51-9
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  • [Title] Hypothalamic hamartoma: basic mechanisms of intrinsic epileptogenesis.
  • The hypothalamic hamartoma (HH) is a rare developmental malformation commonly associated with gelastic seizures that are notoriously refractory to medical therapy.

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  • (PMID = 17544947.001).
  • [ISSN] 1071-9091
  • [Journal-full-title] Seminars in pediatric neurology
  • [ISO-abbreviation] Semin Pediatr Neurol
  • [Language] ENG
  • [Grant] United States / NINDS NIH HHS / NS / R21 NS057786; United States / NINDS NIH HHS / NS / NS044846; United States / NINDS NIH HHS / NS / NS056104
  • [Publication-type] Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Review
  • [Publication-country] United States
  • [Chemical-registry-number] 56-12-2 / gamma-Aminobutyric Acid
  • [Number-of-references] 64
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88. Grynspan D, Meir K, Senger C, Ball NJ: Cutaneous changes in fibrous hamartoma of infancy. J Cutan Pathol; 2007 Jan;34(1):39-43
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  • [Title] Cutaneous changes in fibrous hamartoma of infancy.
  • BACKGROUND: Fibrous hamartoma of infancy (FHI) is a fast growing soft tissue tumor that usually arises in the first 2 years of life.
  • [MeSH-major] Hamartoma / pathology. Skin / pathology. Skin Diseases / pathology

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  • [CommentIn] J Cutan Pathol. 2008 May;35(5):508-9 [18399811.001]
  • (PMID = 17214853.001).
  • [ISSN] 0303-6987
  • [Journal-full-title] Journal of cutaneous pathology
  • [ISO-abbreviation] J. Cutan. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Denmark
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89. López-Laso E, Mateos González ME, Camino León R, Jiménez González MD, Esparza Rodríguez J: Giant hypothalamic hamartoma and dacrystic seizures. Epileptic Disord; 2007 Mar;9(1):90-3
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  • [Title] Giant hypothalamic hamartoma and dacrystic seizures.
  • Ictal crying is a rare type of epileptic seizure associated with hypothalamic hamartoma and with other lesions such as tumours, vascular malformations, hippocampal sclerosis, or cerebral infarction.
  • We describe the case of an infant with gelastic, dacrystic and other types of seizures associated with a giant hypothalamic hamartoma, and present a video sequence of dacrystic seizures.
  • [MeSH-major] Crying. Epilepsy / etiology. Hamartoma / complications. Hypothalamic Neoplasms / complications

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  • (PMID = 17307718.001).
  • [ISSN] 1294-9361
  • [Journal-full-title] Epileptic disorders : international epilepsy journal with videotape
  • [ISO-abbreviation] Epileptic Disord
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] France
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90. Kreiger PA, Ernst LM, Elden LM, Kazahaya K, Alawi F, Russo PA: Hamartomatous tongue lesions in children. Am J Surg Pathol; 2007 Aug;31(8):1186-90
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  • [Title] Hamartomatous tongue lesions in children.
  • The incidence and spectrum of tongue lesions in children, in particular tongue hamartomas, is relatively unknown.
  • We report a retrospective review of all tongue lesions seen at a major tertiary care children's hospital over an 18-year period with an emphasis on describing tongue hamartomas.
  • Interestingly, hamartomatous lesions (18/135) were the third most common lesion category identified.
  • Lingual hamartomas were predominantly submucosal in location and were classified histologically by tissue composition as follows: neurovascular (2/18), smooth muscle predominant (5/18), fat predominant (1/18), and smooth muscle and fat containing (10/18).
  • All 5 smooth muscle predominant hamartomas also contained vasculature, and 1 case additionally contained salivary gland tissue.
  • The single fat predominant hamartoma additionally contained vessels and salivary gland.
  • The final 10 hamartomas contained varying amounts of both smooth muscle and fat, and also admixed combinations of vessels, nerves, and salivary glands.
  • Most patients with hamartomatous lesions were young, 2 years or less.
  • [MeSH-major] Hamartoma / pathology. Tongue Diseases / pathology

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  • (PMID = 17667541.001).
  • [ISSN] 0147-5185
  • [Journal-full-title] The American journal of surgical pathology
  • [ISO-abbreviation] Am. J. Surg. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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91. Cai W, Zhao H, Guo J, Li Y, Yuan Z, Wang W: Retinoic acid-induced lumbosacral neural tube defects: myeloschisis and hamartoma. Childs Nerv Syst; 2007 May;23(5):549-54
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  • [Title] Retinoic acid-induced lumbosacral neural tube defects: myeloschisis and hamartoma.
  • There appeared a dorsally and rostrally situated, neural-plate-like structure (myeloschisis) and a ventrally and caudally located cell mass containing multiple canals (hamartoma) in the lumbosacral NTDs induced by atRA.
  • CONCLUSIONS: Retinoic acid could disturb the notochord and tail bud development in the process of primary and secondary neurulation in rat embryos, which cause lumbosacral NTDs including myeloschisis and hamartoma.
  • [MeSH-major] Abnormalities, Drug-Induced / pathology. Hamartoma / chemically induced. Hamartoma / pathology. Keratolytic Agents / toxicity. Neural Tube Defects / chemically induced. Neural Tube Defects / pathology. Spinal Diseases / chemically induced. Spinal Diseases / pathology. Spine / abnormalities. Teratogens. Tretinoin / toxicity

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  • (PMID = 17252267.001).
  • [ISSN] 0256-7040
  • [Journal-full-title] Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
  • [ISO-abbreviation] Childs Nerv Syst
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Keratolytic Agents; 0 / Teratogens; 5688UTC01R / Tretinoin
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92. Yamura M, Hirai T, Korogi Y, Kitajima M, Hayashida Y, Ikushima I, Endo F, Yamashita Y: Evaluation of small hypothalamic hamartomas with 3D constructive interference in steady state (CISS) sequence. Neuroradiology; 2005 Mar;47(3):204-8
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  • [Title] Evaluation of small hypothalamic hamartomas with 3D constructive interference in steady state (CISS) sequence.
  • Hypothalamic hamartomas are relatively rare, non-neoplastic congenital malformations.
  • With conventional MR images alone, small hypothalamic hamartomas may be difficult to diagnose because of artifacts from cerebrospinal fluid.
  • We present the usefulness of three-dimensional constructive interference in steady state sequence for evaluating small hypothalamic hamartomas in three pediatric patients.
  • [MeSH-major] Hamartoma / diagnosis. Hypothalamic Diseases / diagnosis. Imaging, Three-Dimensional. Magnetic Resonance Imaging

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  • (PMID = 15731910.001).
  • [ISSN] 0028-3940
  • [Journal-full-title] Neuroradiology
  • [ISO-abbreviation] Neuroradiology
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Germany
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93. Jain V, Goel P, Kumar D, Seith A, Sarkar C, Kabra S, Agarwala S: Endobronchial chondroid hamartoma in an infant. J Pediatr Surg; 2009 Sep;44(9):e21-3
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Endobronchial chondroid hamartoma in an infant.
  • The clinical and radiologic findings and management of a rare case of endobronchial chondroid hamartoma in an infant is presented along with a review of the literature.
  • [MeSH-major] Bronchial Neoplasms / diagnosis. Bronchial Neoplasms / surgery. Hamartoma / diagnosis. Hamartoma / surgery

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  • (PMID = 19735804.001).
  • [ISSN] 1531-5037
  • [Journal-full-title] Journal of pediatric surgery
  • [ISO-abbreviation] J. Pediatr. Surg.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 9
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94. Sirinoglu H, Sönmez A, Sav A, Numanoglu A: Lipofibromatous hamartoma of the median nerve. Ann Plast Surg; 2010 Aug;65(2):174-6
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  • [Title] Lipofibromatous hamartoma of the median nerve.
  • Lipofibromatous hamartoma is a rare tumor-like overgrowth of fibroadipose tissue surrounding the nerves.
  • Our case is the first reported case of lipofibromatous hamartoma of the median nerve in the pediatric age group.
  • [MeSH-major] Hamartoma / pathology. Hamartoma / surgery. Lipoma / pathology. Lipoma / surgery. Median Nerve / pathology. Median Nerve / surgery. Peripheral Nervous System Neoplasms / pathology. Peripheral Nervous System Neoplasms / surgery

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  • (PMID = 20606583.001).
  • [ISSN] 1536-3708
  • [Journal-full-title] Annals of plastic surgery
  • [ISO-abbreviation] Ann Plast Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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95. Iida E, Okazaki M, Sarukawa S, Motoi T, Kikuchi Y: Ectopic hamartomatous thymoma growing in the sternocleidomastoid muscle masquerading as sarcoma. Scand J Plast Reconstr Surg Hand Surg; 2006;40(4):249-52
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  • [Title] Ectopic hamartomatous thymoma growing in the sternocleidomastoid muscle masquerading as sarcoma.
  • The distinction between ectopic hamartomatous thymoma and sarcoma is difficult, and preoperative biopsy and intraoperative histopathological examination fail to give a definitive diagnosis.
  • It is important to recognise ectopic hamartomatous thymoma as one of the differential diagnoses of a cervical tumour.

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  • (PMID = 16912001.001).
  • [ISSN] 0284-4311
  • [Journal-full-title] Scandinavian journal of plastic and reconstructive surgery and hand surgery
  • [ISO-abbreviation] Scand J Plast Reconstr Surg Hand Surg
  • [Language] ENG
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
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96. Cheuk W, Lee AK, Arora N, Ben-Arie Y, Chan JK: Splenic hamartoma with bizarre stromal cells. Am J Surg Pathol; 2005 Jan;29(1):109-14
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Splenic hamartoma with bizarre stromal cells.
  • Splenic hamartoma is a rare entity characterized by disorganized red pulp tissue in the absence of interspersed white pulp.
  • It is important to recognize this morphologic variant of splenic hamartoma in order not to misinterpret the bizarre cells as being indicative of a malignancy.
  • [MeSH-major] Hamartoma / pathology. Splenic Diseases / pathology. Stromal Cells / pathology

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  • [CommentIn] Am J Surg Pathol. 2005 Aug;29(8):1114-5 [16006808.001]
  • (PMID = 15613862.001).
  • [ISSN] 0147-5185
  • [Journal-full-title] The American journal of surgical pathology
  • [ISO-abbreviation] Am. J. Surg. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Antigens, CD; 0 / Biomarkers
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97. Tei R, Morimoto T, Miyamoto K, Aketa S, Shimokawara T, Shin Y, Hironaka Y: Intradural extramedullary ganglioneuroma associated with multiple hamartoma syndrome. Neurol Med Chir (Tokyo); 2007 Nov;47(11):513-5
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  • [Title] Intradural extramedullary ganglioneuroma associated with multiple hamartoma syndrome.
  • A 51-year-old woman presented with a rare completely intradural and extramedullary spinal ganglioneuroma associated with multiple hamartoma syndrome and manifesting as complaints of neck pain and dizziness persisting for 8 months.
  • She also suffered from multiple facial trichilemmomas, thyroid goiter, multiple polyposis of the gastrointestinal tract, and pulmonary hamartoma indicating multiple hamartoma syndrome.
  • [MeSH-major] Ganglioneuroma / pathology. Hamartoma Syndrome, Multiple / pathology. Spinal Cord Neoplasms / pathology

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  • (PMID = 18037807.001).
  • [ISSN] 0470-8105
  • [Journal-full-title] Neurologia medico-chirurgica
  • [ISO-abbreviation] Neurol. Med. Chir. (Tokyo)
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
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98. Pawel BR, Crombleholme TM: Mesenchymal hamartoma of the chest wall. Pediatr Surg Int; 2006 Apr;22(4):398-400
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  • [Title] Mesenchymal hamartoma of the chest wall.
  • Mesenchymal hamartoma of the chest wall is an unusual lesion remarkable for its occurrence in early infancy and alarming clinical presentation, which often suggests malignancy.
  • The case of an incompletely resected mesenchymal hamartoma that has behaved in a benign fashion after more than 4 years of follow-up is discussed here.
  • [MeSH-major] Hamartoma / diagnosis. Mesenchymoma / diagnosis. Thoracic Wall / radiography

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  • (PMID = 16331523.001).
  • [ISSN] 0179-0358
  • [Journal-full-title] Pediatric surgery international
  • [ISO-abbreviation] Pediatr. Surg. Int.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
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99. Zbuk KM, Eng C: Hamartomatous polyposis syndromes. Nat Clin Pract Gastroenterol Hepatol; 2007 Sep;4(9):492-502
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Hamartomatous polyposis syndromes.
  • The hamartomatous polyposis syndromes are a heterogeneous group of disorders that share an autosomal-dominant pattern of inheritance and are characterized by hamartomatous polyps of the gastrointestinal tract.
  • These syndromes include juvenile polyposis syndrome, Peutz-Jeghers syndrome and the PTEN hamartoma tumor syndrome.
  • Each hamartomatous polyposis syndrome has its own distinctive organ-specific manifestations and each requires a different surveillance strategy, which makes accurate diagnosis crucial for appropriate patient management.
  • [MeSH-major] Gastrointestinal Neoplasms / diagnosis. Gastrointestinal Neoplasms / physiopathology. Hamartoma Syndrome, Multiple / diagnosis. Hamartoma Syndrome, Multiple / physiopathology. Intestinal Polyposis / diagnosis. Intestinal Polyposis / physiopathology
  • [MeSH-minor] Germ-Line Mutation. Hamartoma. Humans. PTEN Phosphohydrolase / genetics. Peutz-Jeghers Syndrome / diagnosis. Peutz-Jeghers Syndrome / physiopathology. Population Surveillance / methods. Risk Factors

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  • (PMID = 17768394.001).
  • [ISSN] 1743-4386
  • [Journal-full-title] Nature clinical practice. Gastroenterology & hepatology
  • [ISO-abbreviation] Nat Clin Pract Gastroenterol Hepatol
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Review
  • [Publication-country] England
  • [Chemical-registry-number] EC 3.1.3.48 / PTEN protein, human; EC 3.1.3.67 / PTEN Phosphohydrolase
  • [Number-of-references] 79
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100. Hobert JA, Eng C: PTEN hamartoma tumor syndrome: an overview. Genet Med; 2009 Oct;11(10):687-94
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] PTEN hamartoma tumor syndrome: an overview.
  • PTEN hamartoma tumor syndrome (PHTS) encompasses four major clinically distinct syndromes associated with germline mutations in the tumor suppressor PTEN.
  • These allelic disorders, Cowden syndrome, Bannayan-Riley-Ruvalcaba syndrome, Proteus syndrome, and Proteus-like syndrome are associated with unregulated cellular proliferation leading to the formation of hamartomas.
  • Thus far, an increased risk of malignancy has only been documented in Cowden syndrome; however, current recommendations advise that all individuals with PTEN hamartoma tumor syndrome follow the cancer surveillance strategies suggested for Cowden syndrome until further data indicate otherwise.
  • This overview details the clinical description of the PTEN hamartoma tumor syndrome and associated disorders, their diagnosis and molecular/genetic testing, as well as differential diagnosis for assessment of other hamartoma-associated syndromes.
  • [MeSH-major] Hamartoma Syndrome, Multiple / diagnosis. Hamartoma Syndrome, Multiple / genetics






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