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布希克-奥伦多夫综合征:一个日本家族的三代病例

Buschke-Ollendorff syndrome: three generations in a Japanese family.

作者信息

Kawamura Ai, Ochiai Toyoko, Tan-Kinoshita Miyuki, Suzuki Hiroyuki

机构信息

Department of Dermatology, Surugadai Nihon University Hospital, kanda-Surugadai Chiyoda-Ku, Tokyo, Japan.

出版信息

Pediatr Dermatol. 2005 Mar-Apr;22(2):133-7. doi: 10.1111/j.1525-1470.2005.22209.x.

Abstract

Buschke-Ollendorff syndrome is an autosomal dominant disease characterized by disseminated connective tissue nevi of elastic type and osteopoikilosis. We report a 6-year-old Japanese boy with connective tissue nevi that showed slightly grouped yellowish or skin-colored papules and nodules, distributed from birth over his right thigh, right buttock, and back. Radiologic skeletal survey revealed osteopoikilosis. A skin biopsy specimen obtained from a papule showed that collagen bundles in the dermis were thickened and homogenized. The elastic fibers were not increased but were coarse and clumped. The boy's father, at age 34, has had osteopoikilosis and similar papules and nodules on his left buttock and back for the preceding 18 years. We studied the paternal grandfather, aged 65. He had osteopoikilosis and similar skin lesions on his lumbar region. None of the three had a history of hearing loss or malignant tumor. To our knowledge, this is the first report of three generations of Buschke-Ollendorf syndrome in a Japanese family.

摘要

Buschke-Ollendorff综合征是一种常染色体显性疾病,其特征为弹性型播散性结缔组织痣和骨斑点症。我们报告一名6岁日本男孩,其患有结缔组织痣,表现为略呈群集状的淡黄色或肤色丘疹及结节,自出生起分布于右大腿、右臀部及背部。放射学骨骼检查显示有骨斑点症。取自丘疹的皮肤活检标本显示真皮内胶原束增厚且均质化。弹性纤维未增多,但粗大且聚集。该男孩的父亲34岁,在过去18年里,其左臀部及背部有骨斑点症以及类似的丘疹和结节。我们研究了65岁的祖父。他腰椎部位有骨斑点症及类似的皮肤损害。这三人均无听力丧失或恶性肿瘤病史。据我们所知,这是日本一家三代患Buschke-Ollendorf综合征的首例报告。

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