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基内幕细胞痣综合征中具有 D2-40 免疫反应性的皮肤角化囊肿。

Cutaneous Keratocyst With D2-40 Immunoreactivity in Basal Cell Nevus Syndrome.

机构信息

Department of Dermatology, Georgetown University School of Medicine, Washington, DC.

Department of Dermatology, MedStar Washington Hospital Center, Georgetown University Hospital, Washington, DC.

出版信息

Am J Dermatopathol. 2021 Sep 1;43(9):659-661. doi: 10.1097/DAD.0000000000001638.

Abstract

Although not a diagnostic criterion for basal cell nevus syndrome (BCNS, OMIM#109400), cutaneous cysts, particularly epidermoid cysts, are common in this condition. Cutaneous keratocysts, on the other hand, are extremely rare in general and have been identified in only 5 patients with BCNS. Here, we describe a BCNS patient with a cutaneous keratocyst that demonstrated D2-40 (podoplanin) immunoreactivity, which has been detected in odontogenic keratocysts but not cutaneous keratocysts. This finding suggests that cutaneous keratocysts may be developmentally homologous to odontogenic keratocysts and may behave similarly in terms of invasion and growth pattern.

摘要

虽然不是基底细胞痣综合征 (BCNS,OMIM#109400) 的诊断标准,但在这种情况下,皮肤囊肿,特别是表皮样囊肿,很常见。另一方面,皮肤角化囊肿在一般情况下极为罕见,仅在 5 名 BCNS 患者中被发现。在这里,我们描述了一名患有皮肤角化囊肿的 BCNS 患者,该患者的 D2-40(足细胞蛋白)免疫反应阳性,这种情况已在牙源性角化囊肿中检测到,但在皮肤角化囊肿中未检测到。这一发现表明皮肤角化囊肿可能与牙源性角化囊肿在发育上同源,并且在侵袭和生长模式方面可能具有相似的行为。

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