FAMILIAL MULTIPLE TRICHODISCOMAS - A CLINICOPATHOLOGIC STUDY
FAMILIAL MULTIPLE TRICHODISCOMAS - A CLINICOPATHOLOGIC STUDY
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DOI：
10.1001/archderm.121.7.888
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发表时间：
1985-01-01
影响因子：
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通讯作者：
MEIJER, CJLM
中科院分区：
文献类型：
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作者：
STARINK, TM;KISCH, LS;MEIJER, CJLM
例（3）为早发显性遗传的遗传性多发性椎间盘突出。本文分析了27例腰椎间盘瘤的组织学、组织化学、免疫组化及电镜表现。本文对滤泡周围结缔组织肿瘤作一简要回顾，并提出一种分类。遗传性多发性椎间盘瘤是一种新的疾病，应与Birt等描述的以常染色体显性遗传性纤维毛囊瘤为特征的综合征相区别，与椎间盘瘤和软索瘤相关。
Patients (3) had hereditary multiple trichodiscomas of early onset and dominant inheritance. An analysis of the histologic, histochemical, immunohistochemical and EM findings in 27 trichodiscomas, is presented. 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 described by Birt and associates that is characterized by autosomal dominant inherited fibrofolliculomas as the hallmark, associated with trichodiscomas and acrochordons.