布鲁克-斯皮格勒综合征:家族性圆筒状病,一种罕见家族综合征的罕见变体。

Q3 Medicine Case Reports in Dermatological Medicine Pub Date : 2021-06-23 eCollection Date: 2021-01-01 DOI:10.1155/2021/7118260
Harsh Patel, William Naber, Austin Cusick, Craig Oser
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引用次数: 2

摘要

布鲁克-斯皮格勒综合征(BSS)是一种罕见的常染色体显性家族性疾病,导致大量结节附属物的皮肤肿瘤。在这里,我们报告一例家族性柱体病(FC), BSS的一种亚型,患者头皮上最大的柱体为7.4 × 5.6 × 3.8 cm。患者在就诊时患有未确诊的圆筒状瘤,已生长36年;然而,他没有寻求医疗保健评估。来自不同身体部位的三个大肿块的切除和病理调查确定了圆柱体瘤的共同表型。在初次患者切除后,对患者的儿子进行单独评估,也证实了柱状瘤的发展。有新的家族史的患者出现圆筒状瘤的病理证据证实了BSS FC变异的诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Brooke-Spiegler Syndrome: Familial Cylindromatosis, a Rare Variant of a Rare Familial Syndrome.

Brooke-Spiegler Syndrome (BSS) is a rare autosomal dominant familial disorder resulting in dermatologic neoplasms of copious nodular appendages. Here, we report a case of Familial Cylindromatosis (FC), a subtype of BSS, in a patient with the largest cylindroma of 7.4 × 5.6 × 3.8 cm on the scalp. The patient had undiagnosed cylindromas growing for 36 years at presentation; however, he did not seek out healthcare evaluation. Excision and pathologic investigation of three large masses from different body sites determined a shared phenotype of cylindromas. Subsequent evaluation of the patient's son separately, after primary patient excision, confirmed cylindroma development as well. The pathologic evidence of cylindromas in the patient with a new history of family incidence confirmed the diagnosis of the FC variant of BSS.

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CiteScore
1.50
自引率
0.00%
发文量
24
审稿时长
15 weeks
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