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伴有皮脂腺分化的网状棘皮瘤。与穆尔-托里综合征无关。

Reticulated acanthoma with sebaceous differentiation. Lack of association with Muir-Torre syndrome.

作者信息

Haake Dana L, Minni John P, Nowak Michael, Abenoza Pascual, Nousari Carlos H

机构信息

Dermpath Diagnostics South Florida, Pompano Beach, FL 33069, USA.

出版信息

Am J Dermatopathol. 2009 Jun;31(4):391-2. doi: 10.1097/DAD.0b013e318191cafc.

Abstract

We hereby report a case of a reticulated acanthoma with sebaceous differentiation (RASD), a rare and often mislabeled benign lesion that is characterized by epidermal acanthosis and clusters of sebocytes in a reticulated seborrheic keratosis-like pattern. The presence of multiple sebaceous tumors, most notably cystic sebaceous adenomas and keratoacanthomas, has been associated with Muir-Torre syndrome (MTS). Although very rare, cases of RASD have been reported with MTS, which potentially offers profound clinical significance to this neoplasm. This case further supports the lack of association of MTS with RASD.

摘要

我们在此报告一例具有皮脂腺分化的网状棘皮瘤(RASD),这是一种罕见且常被误诊的良性病变,其特征为表皮棘皮症以及呈网状脂溢性角化病样模式的皮脂腺细胞簇。多种皮脂腺肿瘤的存在,最显著的是囊性皮脂腺腺瘤和角化棘皮瘤,与穆尔-托雷综合征(MTS)相关。尽管RASD合并MTS的病例极为罕见,但已有报道,这可能为此肿瘤带来深远的临床意义。本病例进一步支持MTS与RASD之间不存在关联。

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