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皮肤白血病合并格罗弗病

Leukemia cutis in association With Grover's disease.

作者信息

Aldabagh Bishr, Patel Rishi R, Honda Kord

机构信息

Department of Medicine, Akron General Medical Center, Internal Medicine, Akron, OH 44307, USA.

出版信息

Am J Dermatopathol. 2011 Jun;33(4):e41-3. doi: 10.1097/DAD.0b013e3181e7a2f1.

Abstract

Grover's disease (GD), or transient acantholytic dermatosis, is a persistent recurrent dermatosis that usually occurs in men older than 50 years. Rare cases of GD and hematologic malignancy in the same cutaneous biopsy specimen have been reported. We report a case of GD in association with leukemia cutis. A 72-year-old man with a history of myelodysplastic syndrome presented with numerous pruritic papules on the torso, which were clinically diagnosed as GD. A skin biopsy revealed foci of suprabasal acantholysis and dyskeratosis consistent with GD and dense aggregates of mononuclear atypical cells in the superficial dermis consistent with leukemia cutis. Direct immunofluorescence was negative. This case illustrates the need to consider a diagnostic skin biopsy in any patient who presents with classic clinical findings of GD if there is any indication that the patient may be at higher risk for a hematologic malignancy.

摘要

格罗弗病(GD),即暂时性棘层松解性皮病,是一种持续性复发性皮肤病,通常发生于50岁以上男性。同一皮肤活检标本中罕见的GD与血液系统恶性肿瘤并存的病例已有报道。我们报告1例GD合并皮肤白血病的病例。一名有骨髓增生异常综合征病史的72岁男性,躯干出现大量瘙痒性丘疹,临床诊断为GD。皮肤活检显示基底层上棘层松解和角化不良病灶,符合GD表现,真皮浅层有密集的单核非典型细胞聚集,符合皮肤白血病表现。直接免疫荧光检查为阴性。该病例表明,如果有任何迹象显示患者可能有更高的血液系统恶性肿瘤风险,对于任何出现GD典型临床症状的患者,都有必要考虑进行诊断性皮肤活检。

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