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霍奇金病后转化型蕈样肉芽肿的脑膜受累情况。

Meningeal involvement by a transformed mycosis fungoides following Hodgkin's disease.

作者信息

Beylot-Barry M, Dubus P, Vergier B, Cogrel O, Marit G, Beylot C, Merlio J P

机构信息

Department of Dermatology, Hôpital Haut-Lévêque, CHU de Bordeaux et Université de Bordeaux 2, Pessac, France.

出版信息

Br J Dermatol. 1999 Nov;141(5):909-13. doi: 10.1046/j.1365-2133.1999.03168.x.

Abstract

A 58-year-old man had long-standing lesions of presumed large plaque parapsoriasis. Following treatment for nodal Hodgkin's disease (HD), these became more infiltrated, with a diagnosis of mycosis fungoides (MF). A few months later, nodules appeared on the right leg, which was lymphoedematous after inguinal irradiation for HD. Histopathological examination showed CD3+, CD30-, CD15- large pleomorphic lymphocytes, leading to the diagnosis of transformed MF. The cutaneous lesions were successfully treated with topical nitrogen mustard and interferon alfa-2b then methotrexate, but his general health worsened with depression and malaise, without specific neurological symptoms or extracutaneous spreading of the lymphoma. Cerebral computed tomographic scan revealed a cerebellar subdural collection, arachnoid cyst and quadriventricular hydrocephaly, initially considered to be non-specific. After a few weeks, clinical symptoms of intracranial hypertension appeared, and a cerebrospinal fluid (CSF) examination revealed meningeal involvement by the lymphoma. These cells were CD3-negative and the diagnosis was confirmed by polymerase chain reaction (PCR) study, which revealed an identical clonal rearrangement of the T-cell receptor gamma gene between cutaneous biopsies and the CSF. Repeated intrathecal injections of methotrexate and cranial irradiation were performed and the patient was still alive after 13 months. This case illustrates the possible meningeal involvement of MF that may be preceded by atypical and mild neurological or psychiatric symptoms, which may be dissociated from the evolution of the cutaneous lesions. Moreover, PCR study may be useful for both diagnosis and monitoring.

摘要

一名58岁男性长期患有疑似大斑块状副银屑病的皮损。在接受结节性霍奇金病(HD)治疗后,这些皮损浸润加重,诊断为蕈样肉芽肿(MF)。几个月后,右下肢出现结节,该侧下肢在因HD接受腹股沟放疗后出现淋巴水肿。组织病理学检查显示CD3 +、CD30 -、CD15 - 的大的多形性淋巴细胞,从而诊断为转化型MF。皮肤损害通过外用氮芥和干扰素α - 2b,随后使用甲氨蝶呤成功治疗,但患者全身健康状况恶化,出现抑郁和不适,无特定神经症状或淋巴瘤的皮肤外播散。脑部计算机断层扫描显示小脑硬膜下积液、蛛网膜囊肿和四脑室脑积水,最初认为是非特异性的。几周后,出现颅内高压的临床症状,脑脊液(CSF)检查显示淋巴瘤累及脑膜。这些细胞CD3阴性,聚合酶链反应(PCR)研究证实了诊断,该研究显示皮肤活检组织与脑脊液之间T细胞受体γ基因存在相同的克隆重排。反复进行鞘内注射甲氨蝶呤和颅脑放疗,13个月后患者仍存活。该病例说明了MF可能累及脑膜,其之前可能出现非典型和轻微的神经或精神症状,这些症状可能与皮肤损害的演变无关。此外,PCR研究可能对诊断和监测均有用。

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