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Items 1 to 25 of about 25
1. Filipovski V, Banev S, Janevska V, Dukova B: Granular cell tumor of the breast: a case report and review of literature. Cases J; 2009;2:8551

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Granular cell tumor of the breast: a case report and review of literature.
  • Histological evaluation revealed a rare benign neoplasm - granular cell tumor.Granular cell tumor is rare neoplasm that may arise in virtually any body site, and in 5% it occurs in the breast.
  • The histogenesis of this tumor is still rather controversial and currently the most acceptable theory is a Schwann cell origin.
  • The main histological feature is granular cytoplasm of the tumor cells.From a clinical point of view there is a similarity between granular cell tumor and mammary carcinoma on mammography and ultrasound.

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  • (PMID = 19918386.001).
  • [ISSN] 1757-1626
  • [Journal-full-title] Cases journal
  • [ISO-abbreviation] Cases J
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
  • [Other-IDs] NLM/ PMC2769456
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2. Lucendo AJ, De Rezende L, Martín-Plaza J, Larrauri J: Esophageal granular cell tumor and eosinophilic esophagitis: two interesting entities identified in the same patient. Case Rep Gastroenterol; 2008;2(1):33-9

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Esophageal granular cell tumor and eosinophilic esophagitis: two interesting entities identified in the same patient.
  • Endoscopy detected a submucosal tumor in the upper third of the esophagus, which was typified, via biopsy, as a granular cell tumor with benign characteristics and probably responsible for the symptoms.
  • This is the first documented case of the link between granular cell tumors and Eosinophilic esophagitis, two different disorders which could cause dysphagia in young patients.

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  • (PMID = 21490835.001).
  • [ISSN] 1662-0631
  • [Journal-full-title] Case reports in gastroenterology
  • [ISO-abbreviation] Case Rep Gastroenterol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Switzerland
  • [Other-IDs] NLM/ PMC3075163
  • [Keywords] NOTNLM ; Dysphagia / Eosinophilic esophagitis / Esophagus / Granular cell tumors
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3. Wang Y, Li X, Guo Y, Chan L, Guan X: alpha-Lipoic acid increases energy expenditure by enhancing adenosine monophosphate-activated protein kinase-peroxisome proliferator-activated receptor-gamma coactivator-1alpha signaling in the skeletal muscle of aged mice. Metabolism; 2010 Jul;59(7):967-76
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • In addition, metabolic action and cellular signaling of LA were studied in cultured mouse myoblastoma C2C12 cells.

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  • (PMID = 20015518.001).
  • [ISSN] 1532-8600
  • [Journal-full-title] Metabolism: clinical and experimental
  • [ISO-abbreviation] Metab. Clin. Exp.
  • [Language] ENG
  • [Grant] United States / NIDDK NIH HHS / DK / K01 DK075489-04; United States / NIDDK NIH HHS / DK / R03 DK084125; United States / NHLBI NIH HHS / HL / R01 HL051586; United States / NHLBI NIH HHS / HL / HL51586; United States / NIDDK NIH HHS / DK / DK075489-04S1; United States / NHLBI NIH HHS / HL / R01 HL051586-12; United States / NIDDK NIH HHS / DK / K01 DK075489-01; United States / NHLBI NIH HHS / HL / HL051586-12; United States / NIDDK NIH HHS / DK / R03 DK084125-02; United States / NIDDK NIH HHS / DK / DK075489-04; United States / NIDDK NIH HHS / DK / DK075489-01; United States / NIDDK NIH HHS / DK / K01 DK075489-04S1; United States / NIDDK NIH HHS / DK / 5K01DK75489; United States / NIDDK NIH HHS / DK / K01 DK075489; United States / NIDDK NIH HHS / DK / DK084125-02
  • [Publication-type] Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Antioxidants; 0 / Fatty Acids; 0 / Ppargc1a protein, mouse; 0 / Trans-Activators; 0 / Transcription Factors; 47E5O17Y3R / Phenylalanine; 63231-63-0 / RNA; 73Y7P0K73Y / Thioctic Acid; 9G2MP84A8W / Deoxyglucose; EC 2.7.11.11 / Cyclic AMP-Dependent Protein Kinases
  • [Other-IDs] NLM/ NIHMS166156; NLM/ PMC2882509
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4. Joung MK, Lee YJ, Chung CU, Lee JE, Jung SS, Kim SY, Kim JO: A case of granular cell tumor of the trachea. Korean J Intern Med; 2007 Jun;22(2):101-5
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  • [Title] A case of granular cell tumor of the trachea.
  • The pathologic findings showed a benign granular cell tumor.
  • The respiratory symptoms resolved after biopsying the tumor.
  • On follow up, there were no signs of recurrence of the granular cell tumor after a period of 24 months.
  • [MeSH-major] Chest Pain / diagnosis. Granular Cell Tumor / diagnosis. Hemoptysis. Tracheal Neoplasms / diagnosis

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  • (PMID = 17616025.001).
  • [ISSN] 1226-3303
  • [Journal-full-title] The Korean journal of internal medicine
  • [ISO-abbreviation] Korean J. Intern. Med.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Korea (South)
  • [Other-IDs] NLM/ PMC2687619
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5. Basu D, Sengupta A, Adhikari D, Dam A, Anwar T: Granular cell myoblastoma of the tongue in a 2-year-old girl: a case report. J Indian Med Assoc; 2010 Mar;108(3):170, 175
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  • [Title] Granular cell myoblastoma of the tongue in a 2-year-old girl: a case report.
  • Granular cell tumours are uncommon lesions, although the head and neck region accounts for approximately 50% of all lesions.
  • It is not clear whether or not granular cell tumour is a true neoplasm, a developmental anomaly, or a trauma-induced proliferation.
  • The basic cell of origin is now thought to be neural, although past reports frequently indicated an origin from striated muscle, or less frequently an origin from histiocytes, fibroblasts or pericytes.
  • More than a third of all granular cell tumours occur on the lingual dorsum, usually as a sessile, painless, somewhat firm, immoveable nodule less than 1.5 cm in greatest diameter.
  • As most of the granular cell tumours are benign, surgical excision of the lesion is the treatment of choice.
  • [MeSH-major] Granular Cell Tumor / pathology. Tongue Neoplasms / pathology

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  • (PMID = 21043356.001).
  • [ISSN] 0019-5847
  • [Journal-full-title] Journal of the Indian Medical Association
  • [ISO-abbreviation] J Indian Med Assoc
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] India
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6. Arevalo C, Maly B, Eliashar R, Gross M: Laryngeal granular cell tumor. J Voice; 2008 May;22(3):339-42

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Laryngeal granular cell tumor.
  • Granular cell tumor (GCT) of the larynx is an uncommon, benign laryngeal neoplasm.
  • Abrikossoff first described the tumor in 1926 as myoblastoma.
  • The origin of this tumor has been debated in the literature.
  • Most of the authors believe that the tumor is of neural origin due to the characteristic immunohistochemical-staining pattern.
  • The authors describe two cases of laryngeal GCTs located in different sites with a review of the histological and clinical features, the differential diagnosis, and the treatment and the prognosis of the tumor.
  • [MeSH-major] Granular Cell Tumor / diagnosis. Laryngeal Neoplasms / diagnosis. Vocal Cords

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  • (PMID = 17134875.001).
  • [ISSN] 0892-1997
  • [Journal-full-title] Journal of voice : official journal of the Voice Foundation
  • [ISO-abbreviation] J Voice
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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7. Cheewakriangkrai C, Sharma S, Deeb G, Lele S: A rare female genital tract tumor: benign granular cell tumor of vulva: case report and review of the literature. Gynecol Oncol; 2005 May;97(2):656-8
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  • [Title] A rare female genital tract tumor: benign granular cell tumor of vulva: case report and review of the literature.
  • BACKGROUND: The granular cell tumor (GCT) of vulva is a rare female genital tract tumor.
  • Histologic examination of the tumor showed sheets and clusters of infiltrating tumor cells with morphologic features consistent with granular cell tumor.
  • CONCLUSION: Although benign and slow growing, it has a tendency for recurrence and can cause morbidity and mortality when presenting with multicentric or multiple organ involvement due to the lack of effective systemic therapy.
  • [MeSH-major] Granular Cell Tumor / pathology. Vulvar Neoplasms / pathology

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  • (PMID = 15863174.001).
  • [ISSN] 0090-8258
  • [Journal-full-title] Gynecologic oncology
  • [ISO-abbreviation] Gynecol. Oncol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 18
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8. Arican O, Ciralik H, Sasmaz S: Multiple plaques on the back: S-100 negative benign granular cell tumor. J Dermatol; 2005 Jul;32(7):585-8
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  • [Title] Multiple plaques on the back: S-100 negative benign granular cell tumor.
  • Granular cell tumor is a rarely seen disease characterized by a gradually developing nodular lesion, which is difficult to diagnose.
  • The tumor usually appears in the 4th-6th decades of life, more frequently in women and blacks, and has a multifocal location in 10-25% of the cases.
  • The present paper describes an 18-year-old female patient with benign granular cell tumor.
  • This rarely seen type of tumor was S-100 negative and has been detected in biopsies taken from multiple asymptomatic plaques and maculopapular lesions.
  • [MeSH-major] Granular Cell Tumor / pathology. S100 Proteins / analysis. Skin Neoplasms / pathology

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  • (PMID = 16335876.001).
  • [ISSN] 0385-2407
  • [Journal-full-title] The Journal of dermatology
  • [ISO-abbreviation] J. Dermatol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
  • [Chemical-registry-number] 0 / S100 Proteins
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9. Sartorius C, Plechata B, Luis W, Kempf HG: [Granular cell tumor -- a rare tumor lesion of submandibular gland origin]. Laryngorhinootologie; 2005 Oct;84(10):755-7

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  • [Title] [Granular cell tumor -- a rare tumor lesion of submandibular gland origin].
  • [Transliterated title] Granularzelltumor, ein seltener Tumor der Glandula submandibularis.
  • RATIONALE: Granular cell tumors are rare entities with manifestations in nearly all organ systems.
  • CASE REPORT: We report a 54 years old female patient with a painless submandibular tumor lesion.
  • Using a submandibular approach the tumor was totally removed with the submandibular gland.
  • Histologically a benign granular cell tumor was diagnosed.
  • The clinical follow-up for about 3 years was without complications or tumor recidive.
  • CONCLUSIONS: A differential diagnosis of a submandibular mass is the rare manifestation of a benign granular cell tumor.
  • [MeSH-major] Granular Cell Tumor / diagnosis. Submandibular Gland Neoplasms / diagnosis
  • [MeSH-minor] Biomarkers, Tumor / analysis. Diagnosis, Differential. Female. Follow-Up Studies. Humans. Middle Aged. S100 Proteins / analysis. Submandibular Gland / pathology. Submandibular Gland / surgery. Vimentin / analysis

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  • (PMID = 16231244.001).
  • [ISSN] 0935-8943
  • [Journal-full-title] Laryngo- rhino- otologie
  • [ISO-abbreviation] Laryngorhinootologie
  • [Language] ger
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / S100 Proteins; 0 / Vimentin
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10. Rodriguez y Baena R, Di Ieva A, Colombo P, Collini P, Navarria P, Scorsetti M, Gaetani P, Santoro A: Intramedullary astrocytoma with granular cell differentiation. Neurosurg Rev; 2007 Oct;30(4):339-43; discussion 343

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  • [Title] Intramedullary astrocytoma with granular cell differentiation.
  • Granular cell astrocytomas are uncommon tumors of the central nervous system (CNS) of which no cases have been documented in the spinal cord.
  • This variant of glioma should not be confused with benign granular cell tumor which, although rare, has been well characterized in the spinal cord.
  • At surgery, the tumor was found to be infiltrating a posterior column with no dural attachment.
  • The histological diagnosis was astrocytoma with granular cell differentiation.
  • In addition to documenting a unique example of intramedullary granular cell astrocytoma, we review the literature to investigate differences from other tumors with granular changes described in the spinal cord.

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  • (PMID = 17483971.001).
  • [ISSN] 0344-5607
  • [Journal-full-title] Neurosurgical review
  • [ISO-abbreviation] Neurosurg Rev
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
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11. Yilmaz AD, Unlu RE, Orbay H, Sensoz O: Recurrent granular cell tumor: how to treat. J Craniofac Surg; 2007 Sep;18(5):1187-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Recurrent granular cell tumor: how to treat.
  • Granular cell tumor is an uncommon lesion usually located in the head and neck region (50%) with a female sex predominance.
  • Granular cell tumor has a peculiar clinical behavior ranging from clearly benign, locally aggressive, or manifestly malignant.
  • In this article, we present a case of recurrent benign granular cell tumor with the discussion of the treatment modalities.
  • The mass was excised two times at different centers and diagnosed as granular cell tumor after the pathologic examination.
  • [MeSH-major] Granular Cell Tumor / pathology. Head and Neck Neoplasms / pathology. Neoplasm Recurrence, Local / pathology

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  • (PMID = 17912112.001).
  • [ISSN] 1049-2275
  • [Journal-full-title] The Journal of craniofacial surgery
  • [ISO-abbreviation] J Craniofac Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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12. Diel P, Baadners D, Schlüpmann K, Velders M, Schwarz JP: C2C12 myoblastoma cell differentiation and proliferation is stimulated by androgens and associated with a modulation of myostatin and Pax7 expression. J Mol Endocrinol; 2008 May;40(5):231-41
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  • [Title] C2C12 myoblastoma cell differentiation and proliferation is stimulated by androgens and associated with a modulation of myostatin and Pax7 expression.
  • The control of satellite cell activity is a key mechanism during this process.
  • In this study, we analyzed the ability of dihydrotestosterone (DHT) and anabolic steroids to induce and modulate the differentiation of C2C12 myoblastoma cells toward myotubes.
  • The time-dependent effects on differentiation were measured and correlated with the expression of genes involved in the regulation of satellite cell activity.
  • The distribution of C2C12 cells within the cell cycle was measured by flow cytometry and differentiation by creatine kinase (CK) activity.
  • The treatment with DHT and anabolic steroids resulted in a stimulation of C2C12 cell proliferation and CK activity.
  • Our results demonstrate that the key mechanisms of satellite cell differentiation are modulated by androgens.
  • [MeSH-major] Androgens / physiology. Cell Differentiation / physiology. Cell Proliferation. Neoplasms, Muscle Tissue / metabolism. Neoplasms, Muscle Tissue / pathology. PAX7 Transcription Factor / genetics. Transforming Growth Factor beta / genetics
  • [MeSH-minor] Animals. Cell Line, Tumor. Mice. Muscle Fibers, Skeletal / pathology. Myostatin. Satellite Cells, Skeletal Muscle / pathology

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  • [ErratumIn] J Mol Endocrinol. 2014 Aug;53(1):X1
  • (PMID = 18434429.001).
  • [ISSN] 1479-6813
  • [Journal-full-title] Journal of molecular endocrinology
  • [ISO-abbreviation] J. Mol. Endocrinol.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Androgens; 0 / Mstn protein, mouse; 0 / Myostatin; 0 / PAX7 Transcription Factor; 0 / Pax7 protein, mouse; 0 / Transforming Growth Factor beta
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13. Józefowicz-Korczyńska M, Kozłowski Z, Pietruszewska W, Lukomski M: [Granular-cell myoblastoma of the larynx clinical analysis]. Otolaryngol Pol; 2005;59(6):807-12

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Granular-cell myoblastoma of the larynx clinical analysis].
  • Clinical date of four cases of granular-cell myoblastoma tumors arising in the larynx and clinical analysis of 11 cases published in Polish literature were reviewed and studied.
  • Granular-cell tumor is a rare, usually benign neoplasm that can occur in various part of the body.
  • The larynx tumor is accounting for 7% to 10% of all reported cases.
  • The tumor was generally presented in patients in their forth and fifth decade.
  • Clinically the tumors were considered benign.
  • In one case because the location and size of the tumor subtotal laryngectomy was necessary to conduct.
  • [MeSH-major] Granular Cell Tumor / pathology. Laryngeal Neoplasms / pathology

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  • (PMID = 16521442.001).
  • [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; Review
  • [Publication-country] Poland
  • [Number-of-references] 18
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14. Pino Rivero V, Marcos García M, Rejas Ugena E, Trinidad Ruiz G, Pardo Romero G, González Palomino A, Gómez de Tejada Romero R, Blasco Huelva A: [Granular cell tumor of the tongue (Abrikossoff's tumor). Report of a case and review of the literature]. An Otorrinolaringol Ibero Am; 2005;32(1):65-70

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Granular cell tumor of the tongue (Abrikossoff's tumor). Report of a case and review of the literature].
  • [Transliterated title] Tumor de células granulares lingual (tumor de Abrikossoff). Presentación de un caso y revisión de la literatura.
  • Granular cell tumor, myoblastoma or Abrikossoff's tumor is an uncommon benign lesion, usually of slow-growing, that shows a predilection for the oral cavity, especially the tongue.
  • Its real etiopathogenia remains still controversial and in it's histogenesis have been implicated several cell types.
  • [MeSH-major] Granular Cell Tumor / pathology. Tongue Neoplasms / pathology

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  • (PMID = 15803921.001).
  • [ISSN] 0303-8874
  • [Journal-full-title] Anales otorrinolaringológicos ibero-americanos
  • [ISO-abbreviation] An Otorrinolaringol Ibero Am
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article; Review
  • [Publication-country] Spain
  • [Number-of-references] 10
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15. Devi K, Mohanty P, Mohanty L, Bhuyan P, Mishra A, Hazra K: Cytodiagnosis of granular cell tumor: a case report. Indian J Pathol Microbiol; 2007 Jan;50(1):61-2

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Cytodiagnosis of granular cell tumor: a case report.
  • Fine needle aspiration diagnosis was benign granular cell tumor which was confirmed by histopathology.
  • Since it is an uncommon tumor, of controversial histogenesis, it is being reported here.
  • [MeSH-major] Granular Cell Tumor / diagnosis

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  • (PMID = 17474262.001).
  • [ISSN] 0377-4929
  • [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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16. Elakkumanan LB, Chhabra A, Bose S, Sharma K: Granular cell myoblastoma of tongue: a rare cause of unanticipated difficult intubation. Middle East J Anaesthesiol; 2010 Feb;20(4):573-6

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Granular cell myoblastoma of tongue: a rare cause of unanticipated difficult intubation.
  • We report a case of granular cell myoblastoma of the tongue, as a cause of an unanticipated impossible intubation.
  • [MeSH-major] Granular Cell Tumor / pathology. Intubation, Intratracheal / methods. Neoplasms, Muscle Tissue / pathology. Tongue Neoplasms / pathology

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  • (PMID = 20394257.001).
  • [ISSN] 0544-0440
  • [Journal-full-title] Middle East journal of anaesthesiology
  • [ISO-abbreviation] Middle East J Anaesthesiol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Lebanon
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17. Novakov-Mikić A, Ivanović L, Lucić M, Kiralj A, Koprivsek K, Vucković N: [Prenatal diagnosis of granular cell myoblastoma--a case report]. Med Pregl; 2006 Nov-Dec;59(11-12):573-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Prenatal diagnosis of granular cell myoblastoma--a case report].
  • INTRODUCTION: The aim of this paper is to present a case of prenatal diagnosis of a congenital tumor of the oral cavity diagnosed at 28 weeks of gestation.
  • CASE REPORT: After the diagnosis of oral cavity tumor was made by 21) ultrasound, a 3D scan was performed, which confirmed the diagnosis revealing a peduncle at the upper border of maxilla.
  • Magnetic resonance imaging was performed, confirming the diagnosis and the site of the tumor.
  • Regular three-week follow-up scans were performed to follow the growth of the tumor, as well as the state of the amniotic fluid.
  • No tumor growth was detected, and the amniotic fluid volume was normal until 39 weeks of gestation.
  • Cesarean section was scheduled, due to the risk of tumor disruption during a vaginal delivery.
  • The histopathological diagnosis was: granular cell myoblastoma.
  • The female newborn was developing normally, and at 5 months of age there were no traces of scarring at the place of the tumor.
  • [MeSH-major] Granular Cell Tumor / congenital. Mouth Neoplasms / congenital. Mouth Neoplasms / diagnosis

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  • (PMID = 17633900.001).
  • [ISSN] 0025-8105
  • [Journal-full-title] Medicinski pregled
  • [ISO-abbreviation] Med. Pregl.
  • [Language] srp
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Serbia and Montenegro
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18. Kim DH, Murovic JA, Tiel RL, Moes G, Kline DG: A series of 146 peripheral non-neural sheath nerve tumors: 30-year experience at Louisiana State University Health Sciences Center. J Neurosurg; 2005 Feb;102(2):256-66
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • OBJECT: This is a retrospective review of 146 surgically treated benign and malignant peripheral non-neural sheath tumors (PNNSTs).
  • Tumor classifications with patient numbers, locations of benign PNNSTs, and surgical techniques and adjunctive treatments are presented.
  • The results of a literature review regarding tumor frequencies are presented.
  • METHODS: One hundred forty-six patients with 111 benign and 35 malignant PNNSTs were treated between 1969 and 1999 at the Louisiana State University Health Sciences Center (LSUHSC).
  • The benign tumors included 33 ganglion cysts, 16 cases of localized hypertrophic neuropathy, 12 lipomas, 12 tumors of vascular origin, and 11 desmoid tumors.
  • There were four each of lipofibrohamartomas, myositis ossificans, osteochondromas, and ganglioneuromas; two each of meningiomas, cystic hygromas, myoblastoma or granular cell tumors, triton tumors, and lymphangiomas; and one epidermoid cyst.
  • The locations of benign PNNSTs were the following: 33 in the brachial plexus region, 39 in an upper extremity, one in the pelvic plexus, and 38 in a lower extremity.
  • There were two melanomas metastatic to nerve and one tumor each that had metastasized from the bladder, rectum, skin, head and neck, and thyroid, and from a primary Ewing sarcoma.
  • CONCLUSIONS: There were more benign PNNSTs than malignant ones.
  • Benign tumors were relatively equally distributed in the brachial plexus region and upper and lower extremities, with the exception of the pelvic plexus, which had only one tumor.

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  • (PMID = 15739553.001).
  • [ISSN] 0022-3085
  • [Journal-full-title] Journal of neurosurgery
  • [ISO-abbreviation] J. Neurosurg.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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19. Fang HY, Wu CY, Huang HJ, Lin YM: Granular cell tumor of the lung. Lung; 2010 Aug;188(4):355-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Granular cell tumor of the lung.
  • A thoracoscopic RML lobectomy was then performed and immunohistochemical study and Ki-67 proliferative index on the pathology sample demonstrated a benign granular cell tumor.
  • Thirty-six months after surgery, the patient remains symptom-free and there has been no recurrence of the tumor on follow-up CT scan.
  • [MeSH-major] Granular Cell Tumor / diagnostic imaging. Lung Neoplasms / diagnostic imaging

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  • [Cites] Pediatr Pulmonol. 2000 Nov;30(5):425-8 [11064434.001]
  • [Cites] South Med J. 2005 Oct;98(10):1034-5 [16295820.001]
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  • (PMID = 20066540.001).
  • [ISSN] 1432-1750
  • [Journal-full-title] Lung
  • [ISO-abbreviation] Lung
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0Z5B2CJX4D / Fluorodeoxyglucose F18
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20. Stieglitz F, Kitz R, Schäfers HJ, Eickmeier O, Rose M, Fellbaum C, Zielen S: Granular cell tumor of the trachea in a child. Ann Thorac Surg; 2005 Feb;79(2):e15-6

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Granular cell tumor of the trachea in a child.
  • Granular cell tumors are uncommon benign neoplasms.
  • We present the case of a 14-year-old girl with a granular cell tumor of the trachea.
  • The tumor was incidentally found at bronchoscopy performed to exclude suspected foreign body aspiration.
  • Biopsies revealed the histologic pattern of a benign granular cell tumor.
  • She has not had any recurrence of the tumor during 3 years of follow-up.
  • [MeSH-major] Granular Cell Tumor / diagnosis. Granular Cell Tumor / surgery. Tracheal Neoplasms / diagnosis. Tracheal Neoplasms / surgery

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  • (PMID = 15680798.001).
  • [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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21. Cserni G, Bori R, Sejben I: Vascular invasion demonstrated by elastic stain-a common phenomenon in benign granular cell tumors. Virchows Arch; 2009 Feb;454(2):211-5

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Vascular invasion demonstrated by elastic stain-a common phenomenon in benign granular cell tumors.
  • Granular cell tumor is generally benign, but rare malignant cases have been documented.
  • Venous invasion was incidentally identified with the orcein elastic stain in an otherwise benign granular cell tumor (propositus case).
  • Four further benign granular cell tumors were also analyzed; venous invasion was discovered in three.
  • It is suggested that vascular invasion is not uncommon in granular cell tumors and should not lead to the classification of the tumor as malignant or atypical.
  • [MeSH-major] Blood Vessels / pathology. Elastic Tissue / pathology. Granular Cell Tumor / pathology. Staining and Labeling / methods
  • [MeSH-minor] Adult. Aged. Female. Humans. Immunohistochemistry. Lymphatic Metastasis. Male. Neoplasm Invasiveness

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  • [Cites] Dis Colon Rectum. 2007 Nov;50(11):1867-72 [17665249.001]
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  • (PMID = 19066954.001).
  • [ISSN] 1432-2307
  • [Journal-full-title] Virchows Archiv : an international journal of pathology
  • [ISO-abbreviation] Virchows Arch.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Germany
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22. Gajda M, Welzel C, Holzhausen HJ, Jamali Y, Schrom T, Hauptmann S, Bloching M: [Multifocal adult rhabdomyoma of the neck: a rare entity]. Otolaryngol Pol; 2005;59(6):883-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • A review of the world literature revealed about 19 acceptable cases of benign, multifocal adult-type rhabdomyoma with a distinct male predominance.
  • The pathogenesis of this benign striated muscle tumor is still unclear.
  • The differential diagnoses of rhabdomyoma in adults are myoblastoma or Abrikossof tumor, reticulohistiocytoma, rhabdomyosarcoma and hibernoma.
  • Although adult rhabdomyomas have a distinct histology, they often are mistaken for a variety of other lesions, particularly Abrikossof tumor.
  • Light microscopy showed large round to elongated cells with granular, highly eosinophilic cytoplasm, often with peripheral vacuolation.
  • Electron microscopic studies confirmed the tumor's myogenic origin.

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  • (PMID = 16521457.001).
  • [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; Review
  • [Publication-country] Poland
  • [Number-of-references] 16
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23. Miron I, Miron L, Dumitraş S, Aprodu G, Ciobanu A, Tansanu I: [Statistical study of the evolution over ten years of the clinical and therapeutic approach in childhood soft tissue sarcoma]. Rev Med Chir Soc Med Nat Iasi; 2007 Apr-Jun;111(2):358-62
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Based on histological examination 19 cases (32.75%) were of rhabdomyosarcoma type with following subtypes: alveolar--7 patients, embryonic-- 9 cases, fusiform - 2 cases, bothrioid--1 case), 8 cases were undifferentiated soft tissue sarcomas and one patient had a tumor of pleiomorphic type; 13 children (22.41%) had non-rhabdomyosarcoma soft tissue sarcomas: 6 fibrosarcomas, 2 synovial sarcomas, 1 leiomyosarcoma, 1 Kaposi sarcoma, 1 case of malignant peripheral nerve sheath tumor, 1 case of angioma tumor, one liposarcoma; 16 cases were included in soft tissue tumors of uncertain origin (fibromatosis--6 cases, fibrous histiocytoma--4 cases, hamartoma--cases, myoblastoma--1 case, fibro-xanthoma--1 case, hemangioendothelioma--1 case); 1 PPNET (Askin tumor).

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  • (PMID = 17983168.001).
  • [ISSN] 0048-7848
  • [Journal-full-title] Revista medico-chirurgicală̆ a Societă̆ţ̜ii de Medici ş̧i Naturaliş̧ti din Iaş̧i
  • [ISO-abbreviation] Rev Med Chir Soc Med Nat Iasi
  • [Language] rum
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Romania
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24. Angiero F, Crippa R, Stefani M: Granular cells tumour in the oral cavity: report of eleven cases treated with laser surgery. Minerva Stomatol; 2006 Jul-Aug;55(7-8):423-30
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Granular cells tumour in the oral cavity: report of eleven cases treated with laser surgery.
  • METHODS: Between 1999 and 2004, 11 patients (6 females, 5 males; age range 28-66 years) were treated for tumours classified as being of neural origin; they were all myoblastomas or granular cells tumours (ex Abrikossoff tumour).
  • CONCLUSIONS: Granular cell tumour is a benign neoplasm with a tendency to relapse if not completely removed.
  • [MeSH-major] Granular Cell Tumor / surgery. Laser Therapy. Mouth Neoplasms / surgery

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  • (PMID = 17041542.001).
  • [ISSN] 0026-4970
  • [Journal-full-title] Minerva stomatologica
  • [ISO-abbreviation] Minerva Stomatol
  • [Language] eng; ita
  • [Publication-type] Journal Article
  • [Publication-country] Italy
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25. Sobol SE, Samadi DS, Wetmore RF: Pediatric subglottic granular cell myoblastoma. Otolaryngol Head Neck Surg; 2005 Apr;132(4):655-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Pediatric subglottic granular cell myoblastoma.
  • [MeSH-major] Airway Obstruction / etiology. Glottis. Granular Cell Tumor / diagnosis. Laryngeal Neoplasms / diagnosis. Respiratory Sounds / etiology. Tracheal Stenosis / etiology

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  • (PMID = 15806064.001).
  • [ISSN] 0194-5998
  • [Journal-full-title] Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery
  • [ISO-abbreviation] Otolaryngol Head Neck Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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