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一名儿科患者的黑棘皮病与肾上腺皮质肿瘤相关。

Acanthosis nigricans associated with an adrenocortical tumor in a pediatric patient.

作者信息

Isaacoff Elizabeth, Dimitriadi Filippina Filia, Barrows Frank, Pawel Bruce, Mattei Peter, Mostoufi-Moab Sogol

机构信息

Department of Pediatrics, The Children's Hospital of Philadelphia, 34th Street and Civic Center Boulevard, 3535 Market Street, Room 1562, Philadelphia, PA 19104, USA.

出版信息

Case Rep Endocrinol. 2013;2013:174593. doi: 10.1155/2013/174593. Epub 2013 May 30.

Abstract

Malignant acanthosis nigricans (AN) is a rare paraneoplastic syndrome seen primarily in adults with an underlying diagnosis of gastrointestinal adenocarcinoma. Malignant AN is characterized by hyperpigmentation and velvety hyperplasia of the epidermis. This condition is generally not associated with tumors in pediatric populations or in the adrenal gland. We present a case of malignant AN in a pediatric patient with a nonmalignant, functional adrenocortical tumor.

摘要

恶性黑棘皮病(AN)是一种罕见的副肿瘤综合征,主要见于患有胃肠道腺癌的成年人。恶性AN的特征是表皮色素沉着过度和天鹅绒样增生。这种情况通常与儿科人群或肾上腺的肿瘤无关。我们报告一例患有非恶性功能性肾上腺皮质肿瘤的儿科患者发生恶性AN的病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f33e/3683467/0b8132107719/CRIM.ENDOCRINOLOGY2013-174593.001.jpg

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