| Familial multiple trichodiscomas. A clinicopathologic study. | |
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MedLine Citation:
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PMID: 4015134 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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Three patients had hereditary multiple trichodiscomas of early onset and dominant inheritance. This report is an analysis of the histologic, histochemical, immunohistochemical, and electron microscopic findings in 27 trichodiscomas, the largest published series so far, to our knowledge. The tumors of perifollicular connective tissue are briefly reviewed and a classification is proposed. Hereditary multiple trichodiscomas are regarded as a new entity that should be distinguished from the syndrome recently described by Birt and associates that is characterized by autosomal dominant inherited fibrofolliculomas as the hallmark, associated with trichodiscomas and acrochordons. |
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Authors:
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T M Starink; L S Kisch; C J Meijer |
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Publication Detail:
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Type: Case Reports; Journal Article |
Journal Detail:
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Title: Archives of dermatology Volume: 121 ISSN: 0003-987X ISO Abbreviation: Arch Dermatol Publication Date: 1985 Jul |
Date Detail:
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Created Date: 1985-08-07 Completed Date: 1985-08-07 Revised Date: 2008-03-17 |
Medline Journal Info:
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Nlm Unique ID: 0372433 Medline TA: Arch Dermatol Country: UNITED STATES |
Other Details:
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Languages: eng Pagination: 888-91 Citation Subset: AIM; IM |
Export Citation:
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APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
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Adult Aged Female Fibroma / genetics*, pathology Hair / pathology Humans Male Neoplasms, Multiple Primary / genetics*, pathology Skin Neoplasms / genetics*, pathology |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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