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Items 1 to 41 of about 41
1. Swaroop Mr, Nischal Kc, Rajesh Gowda Cm, Umashankar Nu, Basavaraj Hb, Sathyanarayana Bd: Radiofrequency ablation of adenoma sebaceum. J Cutan Aesthet Surg; 2008 Jul;1(2):89-91

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Radiofrequency ablation of adenoma sebaceum.
  • Adenoma sebaceum is one of the diagnostic features of tuberous sclerosis.
  • Histologically, they are angiofibromas that occur over the central part of the face and hence, cause a major cosmetic disfigurement.
  • Laser treatment is expensive and any form of treatment for adenoma sebaceum is not a one-time procedure but is a recurring process as the condition is genetic in aetiology.
  • We hereby report a case of tuberous sclerosis in whom we ablated the lesions by radiofrequency technique with acceptable results.

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  • [Cites] J Dermatol. 2004 Jan;31(1):42-6 [14739503.001]
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  • (PMID = 20300351.001).
  • [ISSN] 0974-5157
  • [Journal-full-title] Journal of cutaneous and aesthetic surgery
  • [ISO-abbreviation] J Cutan Aesthet Surg
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] India
  • [Other-IDs] NLM/ PMC2840910
  • [Keywords] NOTNLM ; Adenoma sebaceum / disfigurement / radiofrequency / tuberous sclerosis
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2. Olubunmi OA: Misdiagnosis of tuberous sclerosis in a Nigerian girl: a case report and review of literature. Ann Afr Med; 2010 Apr-Jun;9(2):95-101
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Misdiagnosis of tuberous sclerosis in a Nigerian girl: a case report and review of literature.
  • Tuberous sclerosis is a rare neuro-cutaneous syndrome, one of the phakomatosis, characterized by facial angiofibromas (adenoma sebaceum), mental retardation and epilepsy.
  • This is a case report of tuberous sclerosis in a 13-year-old Nigerian girl that was misdiagnosed as neurofibromatosis because of her cutaneous lesions.
  • A comprehensive medical clerkship, thorough physical examination, high index of clinical suspicion and neuroimaging investigations are required to confirm diagnosis.
  • [MeSH-major] Brain / radiography. Calcinosis / radiography. Tuberous Sclerosis / radiography
  • [MeSH-minor] Adolescent. Angiofibroma / diagnosis. Anticonvulsants / therapeutic use. Diagnostic Errors. Epilepsy / drug therapy. Epilepsy / etiology. Female. Humans. Intellectual Disability / etiology. Neurofibromatoses / diagnosis. Skin Neoplasms / diagnosis. Tomography, X-Ray Computed. Treatment Outcome. Valproic Acid / therapeutic use

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  • (PMID = 20587932.001).
  • [ISSN] 0975-5764
  • [Journal-full-title] Annals of African medicine
  • [ISO-abbreviation] Ann Afr Med
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] Nigeria
  • [Chemical-registry-number] 0 / Anticonvulsants; 614OI1Z5WI / Valproic Acid
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3. Cabrera Duro A, Rodrigo Carbonero D, Aramendi Gallardo J, Pastor Menchaca E, Galdeano Miranda JM, Hermana Tenzanos T, Prats Viñas JM: [Tuberous sclerosis associated with rhabdomyoma in the left ventricular outlet tract]. An Pediatr (Barc); 2005 Apr;62(4):367-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Tuberous sclerosis associated with rhabdomyoma in the left ventricular outlet tract].
  • [Transliterated title] Esclerosis tuberosa con rabdomioma del tracto de salida del ventrículo izquierdo.
  • We report a 2-month old newborn with a family history of adenoma sebaceum, achromic spots and renal lithiasis.
  • The patient presented multiple seizures 24 hours after surgery with good response to medical therapy.
  • Ten days later, computed tomography showed a spot lesion in the subependimary area in the posterior position of the parietal horn, compatible with a hamartoma associated with tuberous sclerosis.
  • [MeSH-major] Heart Neoplasms / complications. Rhabdomyoma / complications. Tuberous Sclerosis / complications

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  • (PMID = 15826566.001).
  • [ISSN] 1695-4033
  • [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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4. Ghosh SK, Bandyopadhyay D, Chatterjee G, Ghosh A, Sarkar S, Sarkar S: Mucocutaneous changes in tuberous sclerosis complex: a clinical profile of 27 Indian patients. Indian J Dermatol; 2009 Jul;54(3):255-7

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Mucocutaneous changes in tuberous sclerosis complex: a clinical profile of 27 Indian patients.
  • BACKGROUND: Tuberous sclerosis complex (TSC) is an autosomal dominant neurocutaneous disease resulting in a wide array of clinical manifestations, primarily affecting the skin and central nervous system.
  • AIMS: To review the prevalence and patterns of cutaneous manifestations in tuberous sclerosis, in a group of patients from eastern India.
  • METHODS: Observational clinical study on twenty-seven consecutive patients of tuberous sclerosis collected during a period of four years.
  • The classical triad of tuberous sclerosis was present in only nine (33.3%) patients.
  • Adenoma sebaceum was the most common cutaneous feature (100%), followed by hypomelanotic macules (92.6%), connective tissue nevi (66.6%), and Koenen's tumors (33.3%).

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  • [Cites] J Urol. 2003 May;169(5):1635-42 [12686801.001]
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  • (PMID = 20161858.001).
  • [ISSN] 1998-3611
  • [Journal-full-title] Indian journal of dermatology
  • [ISO-abbreviation] Indian J Dermatol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] India
  • [Other-IDs] NLM/ PMC2810693
  • [Keywords] NOTNLM ; Tuberous sclerosis / adenoma sebaceum / mucocutaneous / shagreen patch
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5. Elifritz J, Krishnan RS, Donnelly H: Numerous fibrous papules of the face unassociated with any genodermatosis. Dermatol Online J; 2007;13(4):12

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Numerous fibrous papules of the face unassociated with any genodermatosis.
  • Numerous angiofibromas on the face are commonly associated with tuberous sclerosis or multiple endocrine neoplasia type 1.
  • We present a healthy 66-year-old female with numerous facial angiofibromas, without evidence of tuberous sclerosis, multiple endocrine neoplasia type 1, or any of the less common syndromes associated with many angiofibromas on the face.
  • To our knowledge, there have been no previously reported cases of patients with numerous facial angiofibromas who did not have an associated genodermatosis.
  • [MeSH-major] Angiofibroma / etiology. Facial Neoplasms / etiology
  • [MeSH-minor] Aged. Face. Female. Humans. Skin / pathology. Skin Diseases, Genetic

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  • (PMID = 18319009.001).
  • [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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6. Hori K, Soejima K, Nozaki M, Sakurai H, Takeuchi M, Yamaki T, Iwasaka S, Kono T, Honda T, Isago T: Treatment of facial angiofibroma of tuberous sclerosis using cultured epithelial autografts. Ann Plast Surg; 2006 Oct;57(4):415-7
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  • [Title] Treatment of facial angiofibroma of tuberous sclerosis using cultured epithelial autografts.
  • Treatment of facial angiofibroma of tuberous sclerosis is problematic, because the skin lesions involve entire dermis.
  • Five patients aged from 14 to 33 (mean: 23.6) years old with angiofibroma of tuberous sclerosis were treated with cultured epithelial autografts between 1995 and 2004.
  • The entire area of the facial lesions was excised using a razor to remove large nodules, and then the remaining lesions were further abraded to a rather deep layer of the dermis to smooth the skin and remove small nodules.
  • [MeSH-major] Angiofibroma / surgery. Epithelium / transplantation. Facial Neoplasms / surgery. Tuberous Sclerosis / complications

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  • (PMID = 16998334.001).
  • [ISSN] 0148-7043
  • [Journal-full-title] Annals of plastic surgery
  • [ISO-abbreviation] Ann Plast Surg
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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7. El-Musa KA, Shehadi RS, Shehadi S: Extensive facial adenoma sebaceum: successful treatment with mechanical dermabrasion: case report. Br J Plast Surg; 2005 Dec;58(8):1143-7

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Extensive facial adenoma sebaceum: successful treatment with mechanical dermabrasion: case report.
  • This report documents the successful elimination of disfiguring sebaceous adenomas from the face of a 21-year-old male patient with mechanical dermabrasion.
  • [MeSH-major] Adenoma / surgery. Dermabrasion / methods. Facial Neoplasms / surgery. Sebaceous Gland Neoplasms / surgery

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  • (PMID = 16061214.001).
  • [ISSN] 0007-1226
  • [Journal-full-title] British journal of plastic surgery
  • [ISO-abbreviation] Br J Plast Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
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8. Prabhu S, Mahesh KP: Tuberous sclerosis with oral angiofibroma: case report. Br J Oral Maxillofac Surg; 2010 Apr;48(3):205-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Tuberous sclerosis with oral angiofibroma: case report.
  • Tuberous sclerosis is a multisystem disorder characterised by the formation of hamartomas in various parts of the body.
  • We present a patient who presented with facial angiofibromas (adenoma sebaceum), shagreen patches, and epileptic seizures.
  • Oral papules showed histological features of angiofibroma, which was peculiar to this case.
  • [MeSH-major] Angiofibroma / pathology. Facial Neoplasms / pathology. Mouth Neoplasms / pathology. Tuberous Sclerosis / pathology
  • [MeSH-minor] Adult. Follow-Up Studies. Humans. Male. Skin Neoplasms / pathology

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  • [Copyright] 2009 The British Association of Oral and Maxillofacial Surgeons. Published by Elsevier Ltd. All rights reserved.
  • (PMID = 19640621.001).
  • [ISSN] 1532-1940
  • [Journal-full-title] The British journal of oral & maxillofacial surgery
  • [ISO-abbreviation] Br J Oral Maxillofac Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Scotland
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9. Chen H, Sun XF, Wu JS: [Clinicopathologic study of subependymal giant cell astrocytoma]. Zhonghua Bing Li Xue Za Zhi; 2006 Nov;35(11):656-9
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  • The tumor often occurred in the lateral ventricles (16/18, 88.9%).
  • Eleven patients (61.1%) had clinical features of tuberous sclerosis, usually in the form of facial angiofibroma (8/18, 44.4%).
  • CONCLUSIONS: Subependymal giant cell astrocytoma is a benign brain tumor with distinctive histopathologic features.
  • The tumor typically affects children and young adults.
  • [MeSH-minor] Adolescent. Adult. Child. Female. Follow-Up Studies. Glial Fibrillary Acidic Protein / biosynthesis. Humans. Immunohistochemistry. Magnetic Resonance Imaging. Male. Middle Aged. Retrospective Studies. Synaptophysin / biosynthesis. Tomography, X-Ray Computed. Tuberous Sclerosis / complications. Tuberous Sclerosis / metabolism. Tuberous Sclerosis / pathology. Young Adult

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  • (PMID = 17374208.001).
  • [ISSN] 0529-5807
  • [Journal-full-title] Zhonghua bing li xue za zhi = Chinese journal of pathology
  • [ISO-abbreviation] Zhonghua Bing Li Xue Za Zhi
  • [Language] chi
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] China
  • [Chemical-registry-number] 0 / Glial Fibrillary Acidic Protein; 0 / Synaptophysin
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10. Granata A, Basile A, Figuera M, Mignani R, Fiore CE: Spontaneous retroperitoneal hemorrhage due to massive rupture of renal angiomyolipoma treated with nephrectomy: an unusual onset of tuberous sclerosis complex. Clin Nephrol; 2009 Apr;71(4):441-4
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  • [Title] Spontaneous retroperitoneal hemorrhage due to massive rupture of renal angiomyolipoma treated with nephrectomy: an unusual onset of tuberous sclerosis complex.
  • Tuberous sclerosis complex (TSC) is a genetic and systemic disorder characterized by benign hamartomatous tumors that involve multiple organ systems.
  • The classical clinical triad of TSC consists of seizure, adenoma sebaceum (facial angiofibromata) and mental retardation.
  • Renal angiomyolipomas are documented in approximately 40 - 80% of tuberous sclerosis patients and usually are small and asymptomatic.
  • In these cases diagnosis can be difficult but definitive only after the histological examination or the systemic investigation of other possible tissue involvements.
  • We describe the case of a 28 year old woman who came to the emergency department with acute postprandial abdominal pain and severe anemia due to hemorrhagic renal angiomyolipoma treated by nephrectomy in whom the following examination led to the diagnosis of TSC.
  • [MeSH-major] Angiomyolipoma / complications. Hemorrhage / etiology. Kidney Neoplasms / complications. Retroperitoneal Space. Tuberous Sclerosis / complications
  • [MeSH-minor] Adult. Diagnosis, Differential. Female. Humans. Nephrectomy. Rupture, Spontaneous

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  • (PMID = 19356378.001).
  • [ISSN] 0301-0430
  • [Journal-full-title] Clinical nephrology
  • [ISO-abbreviation] Clin. Nephrol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
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11. Gupta S, Bhowate R, Degwekar SS: Clinical and radiological findings related to tuberous sclerosis complex: a case report. J Contemp Dent Pract; 2008;9(4):85-91
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Clinical and radiological findings related to tuberous sclerosis complex: a case report.
  • AIM: The aim of this report is to present the intraoral and extraoral clinical features of a young female patient with tuberous sclerosis complex (TSC) who exhibited multiple hamartomas of various organ systems including a fibromatous growth on the gingiva.
  • BACKGROUND: TSC is a rare neurocutaneous syndrome exhibiting multiple hamartomatous proliferations that may involve multiple organs such as the brain, kidney, heart, eyes, lungs and skin.
  • Associated findings were adenoma sebaceum (angiofibromas) on the face, a Shagreen patch on the lumbosacral region, ash leaf spots on the trunk, and subangual fibromas (Koenen's tumor) on the nails of fingers and toes.
  • The final diagnosis of TSC was made on the basis of the clinical findings of the skin, computerized tomography (CT) findings of the brain and kidney, ultrasonographic findings of kidney, and a histopathologic evaluation of the gingival growth which met the major and minor criteria required for a diagnosis of TSC.
  • The diagnosis and management of these patients varies depending on the specific presentation of the disease.
  • [MeSH-major] Gingival Diseases / diagnosis. Hamartoma / diagnosis. Tuberous Sclerosis / diagnosis
  • [MeSH-minor] Adolescent. Angiofibroma / diagnosis. Cuspid / pathology. Diagnosis, Differential. Facial Neoplasms / diagnosis. Female. Fibroma / diagnosis. Humans. Hyperpigmentation / diagnosis. Nail Diseases / diagnosis. Skin Neoplasms / diagnosis


12. Umeoka S, Koyama T, Miki Y, Akai M, Tsutsui K, Togashi K: Pictorial review of tuberous sclerosis in various organs. Radiographics; 2008 Nov-Dec;28(7):e32
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Pictorial review of tuberous sclerosis in various organs.
  • Tuberous sclerosis is a rare autosomal dominant neurocutaneous syndrome characterized by the presence of benign congenital tumors in multiple organs.
  • The diagnosis is usually established on the basis of diagnostic criteria applied to physical or radiologic findings.
  • Because the classical triad of epilepsy, mental retardation, and adenoma sebaceum is uncommonly seen at clinical examination, radiologic examinations can play an important role in the diagnosis of tuberous sclerosis and in treatment.
  • Detection of these entities can be strong evidence for suspecting tuberous sclerosis.
  • The presence of pulmonary lymphangioleiomyomatosis, multifocal micronodular pneumocyte hyperplasia, or multiple renal cysts also raises suspicion of tuberous sclerosis.
  • Moreover, tuberous sclerosis can involve bone, liver, and the alimentary tract.
  • Familiarity with the clinical and radiologic findings in various organs is crucial in diagnosis and treatment.
  • [MeSH-major] Multiple Organ Failure / diagnosis. Tomography, X-Ray Computed / methods. Tuberous Sclerosis / diagnosis

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  • (PMID = 18772274.001).
  • [ISSN] 1527-1323
  • [Journal-full-title] Radiographics : a review publication of the Radiological Society of North America, Inc
  • [ISO-abbreviation] Radiographics
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 60
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13. Hall MR, Kovach BT, Miller JL: Unilateral facial angiofibromas without other evidence of tuberous sclerosis: case report and review of the literature. Cutis; 2007 Oct;80(4):284-8
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  • [Title] Unilateral facial angiofibromas without other evidence of tuberous sclerosis: case report and review of the literature.
  • Bilateral facial angiofibromas are common cutaneous manifestations of tuberous sclerosis, an autosomal-dominant disease characterized by hamartomas of multiple organs.
  • Papules in patients with tuberous sclerosis typically appear between 4 and 10 years of age, becoming more extensive during puberty before stabilizing.
  • We present a 28-year-old man with unilateral facial angiofibromas, which may represent a segmental form of tuberous sclerosis.
  • [MeSH-major] Angiofibroma / pathology. Facial Neoplasms / pathology. Skin Neoplasms / pathology. Tuberous Sclerosis / pathology

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  • [ErratumIn] Cutis. 2008 Feb;81(2):155
  • (PMID = 18038689.001).
  • [ISSN] 0011-4162
  • [Journal-full-title] Cutis
  • [ISO-abbreviation] Cutis
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 25
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14. Hunter AG, Nezarati MM, Velsher L: Absence of signs of systemic involvement in four patients with bilateral multiple facial angiofibromas. Am J Med Genet A; 2010 Mar;152A(3):657-64
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Absence of signs of systemic involvement in four patients with bilateral multiple facial angiofibromas.
  • Facial angiofibromas are a major diagnostic sign for tuberous sclerosis (TS) and MEN1, and the former is probably the first disease to be considered by a geneticist when such lesions are found.
  • Early onset facial angiofibromas that are not associated with any other systemic sign appear to be unusual, and their occurrence can leave the clinician with some uncertainty as to their significance, as well as how to proceed.
  • In this article we describe four patients with what appear to be isolated, bilateral facial angiofibromas.
  • We discuss the significance of these lesions with respect to the conditions in which they have been seen, review prior reports of apparently isolated angiofibromas, and provide some rough calculations as to how likely it would be for an underlying systemic condition to be overlooked after different levels of investigation have been performed.
  • [MeSH-major] Angiofibroma / pathology. Facial Neoplasms / pathology. Neoplasms, Multiple Primary / pathology
  • [MeSH-minor] Adolescent. Adult. Age of Onset. DNA Mutational Analysis. Female. Humans. Male. Middle Aged. Multiple Endocrine Neoplasia Type 1 / diagnosis. Multiple Endocrine Neoplasia Type 1 / genetics. Tuberous Sclerosis / diagnosis. Tuberous Sclerosis / genetics

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  • [Copyright] (c) 2010 Wiley-Liss, Inc.
  • (PMID = 20186817.001).
  • [ISSN] 1552-4833
  • [Journal-full-title] American journal of medical genetics. Part A
  • [ISO-abbreviation] Am. J. Med. Genet. A
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 38
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15. Schaffer JV, Gohara MA, McNiff JM, Aasi SZ, Dvoretzky I: Multiple facial angiofibromas: a cutaneous manifestation of Birt-Hogg-Dubé syndrome. J Am Acad Dermatol; 2005 Aug;53(2 Suppl 1):S108-11
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Multiple facial angiofibromas: a cutaneous manifestation of Birt-Hogg-Dubé syndrome.
  • Birt-Hogg-Dubé syndrome (BHDS) is an uncommon autosomal dominant genodermatosis characterized by a triad of skin tumors--fibrofolliculomas, trichodiscomas, and acrochordons--together with an increased risk of renal tumors and spontaneous pneumothoraces.
  • This report describes multiple facial angiofibromas as the predominant initial manifestation of BHDS.
  • The patient had a total of 41 facial papules removed via shave excision, initially for diagnostic and then for therapeutic purposes; histologic evaluation revealed diagnostic features of angiofibroma in 39 lesions and fibrofolliculoma in only 2.
  • BHDS should be considered, along with tuberous sclerosis and multiple endocrine neoplasia type 1, in the differential diagnosis of multiple facial angiofibromas, particularly when onset is in adulthood.
  • [MeSH-major] Angiofibroma / diagnosis. Diseases in Twins / diagnosis. Facial Neoplasms / diagnosis. Neoplastic Syndromes, Hereditary / diagnosis. Skin Neoplasms / diagnosis
  • [MeSH-minor] Adult. Diagnosis, Differential. Genes, Dominant. Humans. Male. Proteins / genetics. Proto-Oncogene Proteins. Tumor Suppressor Proteins. Twins, Monozygotic

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  • (PMID = 16021156.001).
  • [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; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / FLCN protein, human; 0 / Proteins; 0 / Proto-Oncogene Proteins; 0 / Tumor Suppressor Proteins
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16. Weiss ET, Geronemus RG: New technique using combined pulsed dye laser and fractional resurfacing for treating facial angiofibromas in tuberous sclerosis. Lasers Surg Med; 2010 Jul;42(5):357-60
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] New technique using combined pulsed dye laser and fractional resurfacing for treating facial angiofibromas in tuberous sclerosis.
  • BACKGROUND AND OBJECTIVE: Tuberous sclerosis (TS) is a well-described genetic disorder that is classically associated with up to hundreds of facial angiofibromas.
  • Due to the progressive nature of the skin lesions and the early clinical presentation, a safe and effective technique for treating these disfiguring skin lesions is needed.
  • STUDY DESIGN/PATIENTS AND METHODS: We report a combinatorial technique for treating the angiofibromas of TS.
  • RESULTS: In all presented cases, improvement in the number and appearance of facial angiofibromas and erythema is noted.
  • CONCLUSION: The technique of electrosurgery, pulsed-dye laser treatment, and AFR represents a new and safe therapeutic option for treating facial angiofibromas associated with TS.
  • [MeSH-major] Angiofibroma / etiology. Angiofibroma / surgery. Facial Neoplasms / etiology. Facial Neoplasms / surgery. Laser Therapy / methods. Lasers, Dye / therapeutic use. Skin Neoplasms / etiology. Skin Neoplasms / surgery. Tuberous Sclerosis / complications

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  • (PMID = 20583249.001).
  • [ISSN] 1096-9101
  • [Journal-full-title] Lasers in surgery and medicine
  • [ISO-abbreviation] Lasers Surg Med
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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17. Pantelis A, Bootz F, Kühnel T: [Laser skin resurfacing and fibrin sealing as successful treatment for facial angiofibromas in tuberous sclerosis]. HNO; 2007 Dec;55(13):1009-11
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  • [Title] [Laser skin resurfacing and fibrin sealing as successful treatment for facial angiofibromas in tuberous sclerosis].
  • Tuberous sclerosis complex (TSC) is an autosomal-dominant phacomatosis that manifests with visceral harmatomas, epilepsy, and mental retardation.
  • Paranasal angiofibromas may cause bleeding and difficulties in nasal breathing and can stigmatise the individual.
  • [MeSH-major] Angiofibroma / therapy. Debridement / methods. Fibrin Tissue Adhesive / therapeutic use. Laser Therapy / methods. Reconstructive Surgical Procedures / methods. Skin Neoplasms / therapy. Tuberous Sclerosis / therapy


18. Kacerovska D, Vrtel R, Michal M, Vanecek T, Vodicka R, Kreuzberg B, Ricarova R, Pizinger K, Danis D, Reischig T, Kazakov DV: TSC2/PKD1 contiguous gene syndrome: a report of 2 cases with emphasis on dermatopathologic findings. Am J Dermatopathol; 2009 Aug;31(6):532-41
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • The association of tuberous sclerosis complex (TSC) and autosomal dominant polycystic kidney disease (ADPKD), termed TSC2/PKD1 contiguous gene syndrome, is a result of molecular defect demonstrating by deletion disrupting TSC2 and PKD1.
  • Of a total of 13 cutaneous lesions studied, there were 7 facial angiofibromas, 2 shagreen patches, 1 periungual fibroma, 1 hypopigmented macule, 1 epidermoid cyst, and 1 intradermal melanocytic nevus.
  • It is concluded that the histopathological features of skin lesions in this syndrome are similar to those encountered in TSC.
  • [MeSH-major] Polycystic Kidney, Autosomal Dominant / complications. Skin Diseases / pathology. TRPP Cation Channels / genetics. Tuberous Sclerosis / complications. Tumor Suppressor Proteins / genetics

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  • (PMID = 19590422.001).
  • [ISSN] 1533-0311
  • [Journal-full-title] The American Journal of dermatopathology
  • [ISO-abbreviation] Am J Dermatopathol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / TRPP Cation Channels; 0 / Tumor Suppressor Proteins; 0 / polycystic kidney disease 1 protein; 4JG2LF96VF / tuberous sclerosis complex 2 protein
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19. Haq MZ, Dubey I, Khess CR, Das U, Kumar R: Bipolar disorder and tuberous sclerosis complex: is it a mere coincidence? CNS Spectr; 2009 Nov;14(11):643-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Bipolar disorder and tuberous sclerosis complex: is it a mere coincidence?
  • Tuberous sclerosis complex (TSC) is associated with significant psychiatric comorbidity mainly in the form of autistic disorders, hyperkinetic disorders, depression, and anxiety disorders.
  • There are very few reports of bipolar disorder in TSC.
  • The authors present the case of a patient with TSC having bipolar disorder manifesting as manic as well as depressive episodes.
  • The diagnosis of TSC was based on the presence of facial angiofibromas, enamel pits, and shagreen patches on clinical examination, and the presence of cortical tubers and calcified subependymal nodules on neuroimaging.
  • To our knowledge, this is the first report of TSC with bipolar disorder having both manic as well as depressive episodes.
  • The nature of association between TSC and bipolar disorder, and its clinical implications are discussed.
  • [MeSH-major] Bipolar Disorder / etiology. Tuberous Sclerosis / complications


20. Benatiya AI, Bouayed MA, Touiza E, Daoudi K, Mernissi FZ, Tahri H: [Bourneville's tuberous sclerosis. A case report]. J Fr Ophtalmol; 2005 Dec;28(10):e11
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  • [Title] [Bourneville's tuberous sclerosis. A case report].
  • [Transliterated title] La sclérose tubéreuse de Bourneville. A propos d'un cas.
  • INTRODUCTION: Bourneville's tuberous sclerosis (BTS) is an autosomal dominant phakomatosis characterized by the development of a benign hamartoma-like tumor, which is usually located in the skin, kidney, heart, brain, and eyes.
  • We present here a case of a retinal BTS of late diagnosis.
  • Dermatologic examination also showed facial angiofibromas.
  • They are often an incidental diagnosis and evolve slowly.
  • [MeSH-major] Retinal Neoplasms / diagnosis. Tuberous Sclerosis / diagnosis

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  • (PMID = 16395191.001).
  • [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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21. Peces R, Peces C, Cuesta-López E, Pérez-Dueñas V, Vega-Cabrera C, Azorín S, Selgas R: Low-dose rapamycin reduces kidney volume angiomyolipomas and prevents the loss of renal function in a patient with tuberous sclerosis complex. Nephrol Dial Transplant; 2010 Nov;25(11):3787-91
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  • [Title] Low-dose rapamycin reduces kidney volume angiomyolipomas and prevents the loss of renal function in a patient with tuberous sclerosis complex.
  • Tuberous sclerosis complex (TSC) is caused by constitutively activated mammalian target of rapamycin (mTOR) resulting in non-malignant tumours of several organs including renal angiomyolipomas (AMLs).
  • There was also a reduction of facial angiofibromas, improvement of blood pressure control and absence of AML bleeding over this time period.
  • [MeSH-major] Angiomyolipoma / drug therapy. Kidney Neoplasms / drug therapy. Sirolimus / therapeutic use. TOR Serine-Threonine Kinases / antagonists & inhibitors. Tuberous Sclerosis / drug therapy

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  • (PMID = 20663789.001).
  • [ISSN] 1460-2385
  • [Journal-full-title] Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association
  • [ISO-abbreviation] Nephrol. Dial. Transplant.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] England
  • [Chemical-registry-number] EC 2.7.1.1 / TOR Serine-Threonine Kinases; W36ZG6FT64 / Sirolimus
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22. Mentzel T, Kutzner H, Requena L, Hartmann A: [Skin tumors as marker lesions for tumor syndromes]. Pathologe; 2010 Oct;31(6):489-96
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Skin tumors as marker lesions for tumor syndromes].
  • A number of hereditary tumor syndromes are associated with characteristic dermal neoplasms and knowledge and early diagnosis of these lesions may facilitate the diagnostic of the underlying syndrome.
  • These syndromes include Muir-Torre syndrome, associated with cystic sebaceomas, Cowden syndrome, associated with multiple tricholemmomas, Carney complex associated with multiple superficial angiomyxomas, Birt-Hogg-Dubé syndrome associated with multiple fibrofolliculomas, tuberous sclerosis associated with multiple facial angiofibromas and so-called Koenen tumors, patients with renal cell cancer associated with pilar leiomyomatosis and uterine leiomyomas, Gardner syndrome associated with Gardner fibromas and nevoid basal cell carcinoma associated with multiple basal cell carcinomas in young patients.
  • [MeSH-major] Biomarkers, Tumor. Carney Complex / pathology. Skin Neoplasms / pathology
  • [MeSH-minor] Angiofibroma / pathology. Basal Cell Nevus Syndrome / pathology. Birt-Hogg-Dube Syndrome / pathology. Carcinoma, Basal Cell / pathology. Epidermis / pathology. Hamartoma Syndrome, Multiple / pathology. Humans. Kidney Neoplasms / pathology. Leiomyoma / pathology. Male. Muir-Torre Syndrome / pathology. Myxoma / pathology. Syndrome

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  • (PMID = 20960199.001).
  • [ISSN] 1432-1963
  • [Journal-full-title] Der Pathologe
  • [ISO-abbreviation] Pathologe
  • [Language] ger
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Biomarkers, Tumor
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23. Chiarugi M, Martino MC, Pucciarelli M, Decanini L, Vignali C: Recurrent retroperitoneal hemorrhage in a patient with tuberous sclerosis complex: a case report. Cases J; 2008;1(1):424
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Recurrent retroperitoneal hemorrhage in a patient with tuberous sclerosis complex: a case report.
  • BACKGROUND: Tuberous sclerosis complex (TSC) is an autosomal dominant disorder.
  • It is characterized by seizures, mental retardation and hamartomatous lesions, including facial angiofibroma, subependymal giant cell astrocytoma, cardiac rhabdomyoma and renal angiomyolipoma (AML).

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  • [Cites] N Engl J Med. 2008 Jan 10;358(2):140-51 [18184959.001]
  • [Cites] Nephrol Dial Transplant. 2007 Nov;22(11):3330-3 [17717027.001]
  • [Cites] Clin Nephrol. 2006 Jan;65(1):22-7 [16429838.001]
  • [Cites] Am J Kidney Dis. 2006 Jan;47(1):95-102 [16377390.001]
  • [Cites] J Vasc Interv Radiol. 2005 Jan;16(1):45-50 [15640409.001]
  • [Cites] J Urol. 2004 Jan;171(1):102-5 [14665854.001]
  • [Cites] J Urol. 2003 May;169(5):1635-42 [12686801.001]
  • [Cites] Urology. 2008 Nov;72(5):1077-82 [18805573.001]
  • (PMID = 19115994.001).
  • [ISSN] 1757-1626
  • [Journal-full-title] Cases journal
  • [ISO-abbreviation] Cases J
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
  • [Other-IDs] NLM/ PMC2636789
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24. Nuzzo V, Tauchmanová L, Falchetti A, Faggiano A, Marini F, Piantadosi S, Brandi ML, Leopaldi L, Colao A: MEN1 family with a novel frameshift mutation. J Endocrinol Invest; 2006 May;29(5):450-6
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  • Multiple endocrine neoplasm type 1 (MEN1) syndrome predisposes to the development of endocrine and non-endocrine tumors with an autosomal dominant pattern of inheritance.
  • He reported a previous intestinal resection for bowel occlusion with a histological diagnosis of unspecified mesenchymal neoplasia.
  • He had also undergone a left adrenalectomy for a large nonfunctioning adrenal adenoma.
  • On physical examination, multiple abdominal cutaneous lipomas and facial angiofibromas were observed.
  • [MeSH-major] Frameshift Mutation / genetics. Multiple Endocrine Neoplasia Type 1 / genetics

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  • (PMID = 16794369.001).
  • [ISSN] 0391-4097
  • [Journal-full-title] Journal of endocrinological investigation
  • [ISO-abbreviation] J. Endocrinol. Invest.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Italy
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25. Timotin L, Sarrot-Reynauld F, Lantuejoul S, Pasquier B, Massot C, Ashraf A, Borgel F: [Tuberous sclerosis without mental impairment, diagnosed in adulthood]. Rev Med Interne; 2005 Jun;26(6):511-3
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Tuberous sclerosis without mental impairment, diagnosed in adulthood].
  • [Transliterated title] Sclérose tubéreuse de Bourneville sans altération intellectuelle, diagnostiquée à l'âge adulte.
  • INTRODUCTION: Tuberous sclerosis complex (TSC) is an autosomal dominant inherited phakomatosis, usually diagnosed in childhood and characterized by cutaneous and neurological tumors, the latter often leading to epilepsy and mental retardation.
  • EXEGESIS: We report a case of TSC diagnosed in a 33-year-old man, without any known family history of phakomatosis, presenting with facial angiofibromas, hypomelanotic macules, a giant-cell astrocytoma and retinal phakomas without any mental impairment or epilepsy.
  • CONCLUSION: TSC may occur in patients who do not have any family history of phakomatosis because de novo mutations are frequent.
  • Facial angiofibromas are highly suggestive of tuberous sclerosis complex.

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  • (PMID = 15936480.001).
  • [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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26. Sun XF, Yan CL, Fang L, Shen FM, Liao KH: Cutaneous lesions and visceral involvement of tuberous sclerosis. Chin Med J (Engl); 2005 Feb 5;118(3):215-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Cutaneous lesions and visceral involvement of tuberous sclerosis.
  • BACKGROUND: Tuberous sclerosis (TS) is an autosomal dominant disorder with a significant range of clinical expressions.
  • RESULTS: The skin, brain and kidney were involved frequently in TS patients.
  • They were followed by facial angiofibromas and Shangreen's patch in a decreasing frequency.
  • Forehead plaque, facial angiofibromas and Shagreen's patch appeared in patients at mean age of 2.6, 6.0 and 8.1 years respectively.
  • CONCLUSIONS: Cutaneous features of TS are helpful in the early diagnosis of the disease.
  • Cranial CT is of great value in the diagnosis of TS.
  • [MeSH-major] Skin / pathology. Tuberous Sclerosis / pathology

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  • (PMID = 15740650.001).
  • [ISSN] 0366-6999
  • [Journal-full-title] Chinese medical journal
  • [ISO-abbreviation] Chin. Med. J.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] China
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27. Muhammed K, Mathew J: Coexistence of two neurocutaneous syndromes: tuberous sclerosis and hypomelanosis of Ito. Indian J Dermatol Venereol Leprol; 2007 Jan-Feb;73(1):43-5
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  • [Title] Coexistence of two neurocutaneous syndromes: tuberous sclerosis and hypomelanosis of Ito.
  • Tuberous sclerosis complex (TSC) and hypomelanosis of Ito (HI) are two uncommon neurocutaneous syndromes and their coexistence is extremely rare.
  • An epileptic child presented with progressively increasing multiple hypopigmented macules arranged in a linear and whorled pattern along the lines of Blaschko over the trunk and limbs, characteristic of HI.
  • He also had facial angiofibromas, ash-leaf and confetti macules and shagreen patches.
  • [MeSH-major] Hypopigmentation / complications. Tuberous Sclerosis / complications
  • [MeSH-minor] Angiofibroma / complications. Brain / pathology. Child, Preschool. Epilepsy / complications. Facial Neoplasms / complications. Humans. Intellectual Disability / complications. Magnetic Resonance Imaging. Male

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  • (PMID = 17314448.001).
  • [ISSN] 0973-3922
  • [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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28. Assefa G, Alemie B: Tuberous sclerosis complex (TSC) and Klippel-Trenaunay-Weber (KTW) syndromes association of two complete phakomatoses in a single individual. Ethiop Med J; 2010 Oct;48(4):315-20
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  • [Title] Tuberous sclerosis complex (TSC) and Klippel-Trenaunay-Weber (KTW) syndromes association of two complete phakomatoses in a single individual.
  • Tuberous sclerosis or tuberous sclerosis complex (TSC) and Klippel-Trenaunay-Weber (KTW) syndromes are phakomatoses which are believed to be inherited separately were associated in a 21 years old female, with no family history of similar illness presented with facial rash of reddish spots or bumps, facial angiofibroma (adenoma cebaceum), which appeared on the nose and cheeks in a butterfly distribution, and sub ependymal calcific nodules on brain CT, and multiple liver, pancreas hamartomas and multiple angiomyolipomas and cysts of both kidney on ultrasound, which is consistent with a sporadic TSC, in addition, the diagnostic triad of KTW involved the left upper limb : cutaneous naevi a vascular anomaly, soft tissue and osteohypertrophy.
  • [MeSH-major] Klippel-Trenaunay-Weber Syndrome / complications. Tuberous Sclerosis / complications

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  • (PMID = 21280434.001).
  • [ISSN] 0014-1755
  • [Journal-full-title] Ethiopian medical journal
  • [ISO-abbreviation] Ethiop. Med. J.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Ethiopia
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29. Jóźwiak J, Galus R: Molecular implications of skin lesions in tuberous sclerosis. Am J Dermatopathol; 2008 Jun;30(3):256-61
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  • [Title] Molecular implications of skin lesions in tuberous sclerosis.
  • Tuberous sclerosis (TS), neurocutaneous disorder resulting from the mutation of 1 of 2 genes, TSC1 or TSC2, is often associated with the formation of hamartomatous lesions in various organ systems, including the skin.
  • TS patients may present with hypomelanic macules, confetti-like spots, facial angiofibromas, ungual fibromas, shagreen patches, forehead plaques, and other dermatological signs.
  • Some of these manifestations are pathognomic for TS and thus should be carefully evaluated when TS diagnosis is suspected.
  • In the current review, we describe molecular pathways thought to be responsible for the development of the disease and show how their upregulation may affect the skin.
  • [MeSH-major] Proto-Oncogene Proteins c-akt / genetics. Skin Diseases / genetics. Tuberous Sclerosis / genetics


30. Septer S, Thompson ES, Willemsen-Dunlap A: Anesthesia concerns for children with tuberous sclerosis. AANA J; 2006 Jun;74(3):219-25
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Anesthesia concerns for children with tuberous sclerosis.
  • Tuberous sclerosis (TS) is a relatively rare, autosomal dominant syndrome that displays high genetic penetrance in affected families.
  • It is identified by a classic triad of symptoms including epilepsy, skin lesions, and mental retardation.
  • Tuberous sclerosis causes hamartomas in multiple organ systems, including the brain, skin, heart, kidneys, lungs, and liver.
  • We describe a 10-year-old girl with TS scheduled to receive a general anesthetic for laser treatment of facial angiofibromas.
  • The patient had several coexisting maladies from TS, including hypertension, autism, seizure disorder, cardiac rhabdomyomas, developmental delay, and bilateral polycystic renal disease.
  • [MeSH-major] Anesthesia, General / methods. Tuberous Sclerosis / surgery
  • [MeSH-minor] Angiofibroma / etiology. Angiofibroma / surgery. Child. Developmental Disabilities / etiology. Echocardiography. Facial Neoplasms / etiology. Facial Neoplasms / surgery. Female. Genes, Dominant / genetics. Heart Neoplasms / etiology. Heart Neoplasms / ultrasonography. Humans. Hypertension / etiology. Incidence. Laser Therapy. Nursing Assessment. Patient Care Planning. Penetrance. Perioperative Care / methods. Perioperative Care / nursing. Polycystic Kidney Diseases / etiology. Rare Diseases. Rhabdomyoma / etiology. Rhabdomyoma / ultrasonography. Seizures / etiology

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  • (PMID = 16786916.001).
  • [ISSN] 0094-6354
  • [Journal-full-title] AANA journal
  • [ISO-abbreviation] AANA J
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 50
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31. Rauktys A, Lee N, Lee L, Dabora SL: Topical rapamycin inhibits tuberous sclerosis tumor growth in a nude mouse model. BMC Dermatol; 2008;8:1
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Topical rapamycin inhibits tuberous sclerosis tumor growth in a nude mouse model.
  • BACKGROUND: Skin manifestations of Tuberous Sclerosis Complex (TSC) cause significant morbidity.
  • RESULTS: Treatment with topical rapamycin improved survival and reduced tumor growth.
  • CONCLUSION: Topical rapamycin inhibits TSC-related tumor growth.
  • These findings could lead to a novel treatment approach for facial angiofibromas and other TSC skin lesions.
  • [MeSH-major] Antibiotics, Antineoplastic / administration & dosage. Enzyme Inhibitors / administration & dosage. Protein Kinases / drug effects. Sirolimus / administration & dosage. Soft Tissue Neoplasms / drug therapy. Tuberous Sclerosis / drug therapy
  • [MeSH-minor] Administration, Cutaneous. Animals. Cell Line, Tumor. Disease Models, Animal. Mice. Mice, Nude. Neoplasm Transplantation. Skin Absorption. Survival Analysis. TOR Serine-Threonine Kinases

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  • (PMID = 18226258.001).
  • [ISSN] 1471-5945
  • [Journal-full-title] BMC dermatology
  • [ISO-abbreviation] BMC Dermatol.
  • [Language] eng
  • [Grant] United States / NIDDK NIH HHS / DK / R01 DK066366
  • [Publication-type] Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Antibiotics, Antineoplastic; 0 / Enzyme Inhibitors; EC 2.7.- / Protein Kinases; EC 2.7.1.1 / TOR Serine-Threonine Kinases; EC 2.7.1.1 / mTOR protein, mouse; W36ZG6FT64 / Sirolimus
  • [Other-IDs] NLM/ PMC2266897
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32. Hofbauer GF, Marcollo-Pini A, Corsenca A, Kistler AD, French LE, Wüthrich RP, Serra AL: The mTOR inhibitor rapamycin significantly improves facial angiofibroma lesions in a patient with tuberous sclerosis. Br J Dermatol; 2008 Aug;159(2):473-5
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] The mTOR inhibitor rapamycin significantly improves facial angiofibroma lesions in a patient with tuberous sclerosis.
  • Tuberous sclerosis complex (TSC) is an autosomal dominant disorder with an incidence of approximately one in 6000.
  • Angiofibroma affects 70-80% of patients with TSC, typically on the face.
  • Immunosuppressive treatment with rapamycin, a specific mTOR inhibitor, initiated because of renal transplantation, reduced facial angiofibroma dramatically.
  • [MeSH-major] Angiofibroma / drug therapy. Facial Neoplasms / drug therapy. Sirolimus / therapeutic use. Skin Neoplasms / drug therapy. Tuberous Sclerosis / complications


33. Grieb S, Kruse R, Bruch-Gerharz D, Reifenberger J: [Tuberous sclerosis: diagnostic criteria and new treatment approaches]. Hautarzt; 2008 Oct;59(10):774-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Tuberous sclerosis: diagnostic criteria and new treatment approaches].
  • With a prevalence of 1 in 6,000 births, tuberous sclerosis is a relatively frequent hamartoma and tumor syndrome inherited as an autosomal dominant trait, which manifests primarily on the skin and in the central nervous system.
  • Treatment for many years consisted solely in using nonspecific symptomatic approaches; dermatological therapy comprised mainly laser or electroacoustic ablation of facial angiofibromas.
  • New models of therapy hinder the pathogenesis of tuberous sclerosis.
  • [MeSH-major] Dermatologic Agents / therapeutic use. Interferon-gamma / therapeutic use. Skin Diseases / diagnosis. Skin Diseases / drug therapy. Tuberous Sclerosis / diagnosis. Tuberous Sclerosis / drug therapy

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  • (PMID = 18806968.001).
  • [ISSN] 1432-1173
  • [Journal-full-title] Der Hautarzt; Zeitschrift für Dermatologie, Venerologie, und verwandte Gebiete
  • [ISO-abbreviation] Hautarzt
  • [Language] ger
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Dermatologic Agents; 0 / Recombinant Proteins; 82115-62-6 / Interferon-gamma
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34. Sakuma T, Ueno C, Kawano K: [Sebaceous adenoma of caruncula lacrimalis: report of two cases]. Klin Monbl Augenheilkd; 2009 May;226(5):432-3
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  • [Title] [Sebaceous adenoma of caruncula lacrimalis: report of two cases].
  • [Transliterated title] Adenoma Sebaceum der Caruncula Lacrimalis: Bericht über zwei Fälle.

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  • (PMID = 19507089.001).
  • [ISSN] 1439-3999
  • [Journal-full-title] Klinische Monatsblätter für Augenheilkunde
  • [ISO-abbreviation] Klin Monbl Augenheilkd
  • [Language] ger
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
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35. Sakurai A, Hashizume K, Fukushima Y: Facial angiofibroma as an initial manifestation in multiple endocrine neoplasia type 1. Intern Med; 2008;47(11):1067-8
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  • [Title] Facial angiofibroma as an initial manifestation in multiple endocrine neoplasia type 1.
  • [MeSH-major] Angiofibroma / pathology. Facial Neoplasms / pathology. Multiple Endocrine Neoplasia Type 1 / diagnosis

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  • (PMID = 18520124.001).
  • [ISSN] 1349-7235
  • [Journal-full-title] Internal medicine (Tokyo, Japan)
  • [ISO-abbreviation] Intern. Med.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
  • [Chemical-registry-number] 0 / MEN1 protein, human; 0 / Proto-Oncogene Proteins
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36. Hemady N, Ohri S: Papulonodular lesions in a man with seizures and mental retardation. Adenoma sebaceum. Am Fam Physician; 2009 Jan 1;79(1):48, 51
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  • [Title] Papulonodular lesions in a man with seizures and mental retardation. Adenoma sebaceum.
  • [MeSH-major] Adenoma / pathology. Intellectual Disability / complications. Sebaceous Gland Neoplasms / pathology. Seizures / complications

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  • (PMID = 19145966.001).
  • [ISSN] 0002-838X
  • [Journal-full-title] American family physician
  • [ISO-abbreviation] Am Fam Physician
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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37. Schepis C, Siragusa M: Cryosurgery: an easy and cheap therapy for facial angiofibromas in tuberous sclerosis. Eur J Dermatol; 2010 Jul-Aug;20(4):506-7
MedlinePlus Health Information. consumer health - Tuberous Sclerosis.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Cryosurgery: an easy and cheap therapy for facial angiofibromas in tuberous sclerosis.
  • [MeSH-major] Angiofibroma / surgery. Cryosurgery / methods. Facial Neoplasms / surgery. Tuberous Sclerosis / surgery

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  • (PMID = 20403796.001).
  • [ISSN] 1167-1122
  • [Journal-full-title] European journal of dermatology : EJD
  • [ISO-abbreviation] Eur J Dermatol
  • [Language] eng
  • [Publication-type] Case Reports; Letter
  • [Publication-country] France
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38. Bordel-Gómez MT, Monteagudo-Sánchez B, Alvarez-Fernández JC: [Multiple unilateral facial angiofibromas: description of a new case]. Actas Dermosifiliogr; 2008 Dec;99(10):824-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Multiple unilateral facial angiofibromas: description of a new case].
  • [Transliterated title] Angiofibromas faciales múltiples unilaterales: aportación de un nuevo caso.
  • [MeSH-major] Angiofibroma / genetics. Facial Neoplasms / genetics. Tuberous Sclerosis / diagnosis
  • [MeSH-minor] Adult. Calcium Phosphates / therapeutic use. Female. Glycopeptides / therapeutic use. Humans. Immunocompromised Host. Multiple Sclerosis / complications. Multiple Sclerosis / drug therapy

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  • (PMID = 19091228.001).
  • [ISSN] 0001-7310
  • [Journal-full-title] Actas dermo-sifiliográficas
  • [ISO-abbreviation] Actas Dermosifiliogr
  • [Language] spa
  • [Publication-type] Case Reports; Letter; Review
  • [Publication-country] Spain
  • [Chemical-registry-number] 0 / Calcium Phosphates; 0 / Glycopeptides; 87139-86-4 / Immunoferon
  • [Number-of-references] 16
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39. Haemel AK, O'Brian AL, Teng JM: Topical rapamycin: a novel approach to facial angiofibromas in tuberous sclerosis. Arch Dermatol; 2010 Jul;146(7):715-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Topical rapamycin: a novel approach to facial angiofibromas in tuberous sclerosis.
  • [MeSH-major] Angiofibroma / drug therapy. Facial Neoplasms / drug therapy. Immunosuppressive Agents / administration & dosage. Sirolimus / administration & dosage. Tuberous Sclerosis / complications
  • [MeSH-minor] Administration, Topical. Adolescent. Cheek. Diagnosis, Differential. Female. Follow-Up Studies. Humans

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  • [CommentIn] JAMA Dermatol. 2013 Feb;149(2):203 [23426474.001]
  • [CommentIn] Arch Dermatol. 2011 Sep;147(9):1116-7 [21931059.001]
  • (PMID = 20644030.001).
  • [ISSN] 1538-3652
  • [Journal-full-title] Archives of dermatology
  • [ISO-abbreviation] Arch Dermatol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Immunosuppressive Agents; W36ZG6FT64 / Sirolimus
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40. Türkmen M, Ertam I, Unal I, Dereli T: Facial angiofibromas of tuberous sclerosis: successful treatment with podophyllin. J Eur Acad Dermatol Venereol; 2009 Jun;23(6):713-4
MedlinePlus Health Information. consumer health - Tuberous Sclerosis.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Facial angiofibromas of tuberous sclerosis: successful treatment with podophyllin.
  • [MeSH-major] Angiofibroma / drug therapy. Face. Podophyllin / therapeutic use. Tuberous Sclerosis / complications

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  • (PMID = 18785889.001).
  • [ISSN] 1468-3083
  • [Journal-full-title] Journal of the European Academy of Dermatology and Venereology : JEADV
  • [ISO-abbreviation] J Eur Acad Dermatol Venereol
  • [Language] eng
  • [Publication-type] Case Reports; Letter
  • [Publication-country] Netherlands
  • [Chemical-registry-number] 9000-55-9 / Podophyllin
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41. Camprubí M, Balaguer A, Azon Masoliver A, Jiménez-Feijoo R, Escribano Subias J: Unilateral facial angiofibromas; a review of the literature. Pediatr Dermatol; 2006 May-Jun;23(3):303-5
MedlinePlus Health Information. consumer health - Skin Cancer.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Unilateral facial angiofibromas; a review of the literature.
  • [MeSH-major] Angiofibroma / pathology. Facial Neoplasms / pathology. Skin Neoplasms / pathology
  • [MeSH-minor] Adolescent. Humans. Male. Tuberous Sclerosis / complications

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  • (PMID = 16780491.001).
  • [ISSN] 0736-8046
  • [Journal-full-title] Pediatric dermatology
  • [ISO-abbreviation] Pediatr Dermatol
  • [Language] eng
  • [Publication-type] Case Reports; Letter; Review
  • [Publication-country] United States
  • [Number-of-references] 11
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