Osuji Nnenna, Fearfield Louise, Matutes Estella, Wotherspoon Andrew C, Bunker Christopher, Catovsky Daniel
Academic Department of Haematology and Cytogenetics, Royal Marsden Hospital, London, UK.
Br J Haematol. 2003 Oct;123(2):297-304. doi: 10.1046/j.1365-2141.2003.04592.x.
Granulomatous slack skin disease (GSSD) is a rare condition characterized clinically by redundant skin folds, which show a predilection towards flexural areas, and histologically by a granulomatous T-cell infiltrate and loss of elastic fibres. The disease is often indolent, although rapid progression and transformation have been described. There is much debate as to whether this condition is a subset of mycosis fungoides or a separate disease entity in itself. We describe a case of GSSD with unique manifestations including granulomatous bone marrow involvement and hypercalcaemia. The patient has twice achieved a good response to pentostatin after failure of combination chemotherapy. This is the first report of the successful use of the purine analogue pentostatin in the management of GSSD.
肉芽肿性皮肤松弛症(GSSD)是一种罕见疾病,临床特征为皮肤褶皱过多,好发于屈侧部位,组织学表现为肉芽肿性T细胞浸润和弹性纤维缺失。该疾病通常进展缓慢,不过也有快速进展和转变的报道。关于这种疾病是蕈样肉芽肿的一个亚型还是一种独立的疾病实体,存在诸多争议。我们报告一例具有独特表现的GSSD病例,包括肉芽肿性骨髓受累和高钙血症。该患者在联合化疗失败后,两次使用喷司他丁均取得了良好疗效。这是关于嘌呤类似物喷司他丁成功用于治疗GSSD的首例报道。