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噬血细胞综合征与转移性黑色素瘤:3例报告

[Hemophagocytic syndrome and metastatic melanoma: 3 cases].

作者信息

Cordel N, Le Corvaisier-Piéto C, Young P, Lenormand B, Courville P, Soubrane J, Joly P, Lauret P

机构信息

Clinique Dermatologique, CHU de Rouen.

出版信息

Ann Dermatol Venereol. 2000 Dec;127(12):1077-9.

Abstract

BACKGROUND

Macrophage activation syndrome was initially described during viral infections in immunocompromised patients. Since the original report, many diseases have been found to be associated with macrophage activation syndrome. Lymphoproliferative disorders have been more frequently reported to be associated with macrophage activation syndrome than solid tumors. We herein report three cases of macrophage activation syndrome in patients with metastatic malignant melanoma.

CASE-REPORTS: Two young 32 and 40 year-old men with a liver metastatic malignant melanoma and a 62 year-old woman with a polymetastatic malignant melanoma presented a sudden deterioration of general health with hyperthermia and biological abnormalities: liver cytolysis, leucocytosis, thrombocytopenia, hypertriglyceridaemia. A fatal clinical outcome occurred rapidly despite corticotherapy and/or chemotherapy. For the first two patients the macrophage activation syndrome diagnosis was delayed because of the similarities of macrophage activation syndrome and metastatic malignant melanoma symptoms.

DISCUSSION

The diagnosis of macrophage activation syndrome in patients with metastatic malignant melanoma may be difficult because of the similarities between clinical features of macrophage activation syndrome and those of metastatic malignant melanoma. Hypertriglyceridaemia is present in 60 p. 100 of macrophage activation syndrome and should lead to process a bone marrow aspirate. The search for a triggering infection should be systematically carry out because it is implicated in more than half of macrophage activation syndrome whatever the associated disease may be: neoplasia, autoimmune disease. The pathogenesis of macrophage activation syndromes occurring in patients with metastatic cancer remains unexplained. Treatment of macrophage activation syndrome is not unanimously established and usually consists in the treatment of the associated condition as well as a corticosteroid and/or an immunosuppressive treatment regimens. Prognosis of macrophage activation syndrome is usually poor especially when it is associated with a neoplasia since a fatal outcome occurs in 40 to 60 p. 100 of cases.

摘要

背景

巨噬细胞活化综合征最初是在免疫功能低下患者的病毒感染期间被描述的。自最初报道以来,已发现许多疾病与巨噬细胞活化综合征相关。与实体瘤相比,淋巴增殖性疾病与巨噬细胞活化综合征的相关性报道更为频繁。我们在此报告三例转移性恶性黑色素瘤患者发生巨噬细胞活化综合征的病例。

病例报告

两名分别为32岁和40岁的患有肝转移性恶性黑色素瘤的年轻男性以及一名62岁的患有多部位转移性恶性黑色素瘤的女性,出现了全身健康状况的突然恶化,伴有高热和生物学异常:肝细胞溶解、白细胞增多、血小板减少、高甘油三酯血症。尽管进行了皮质类固醇治疗和/或化疗,但仍迅速出现了致命的临床结局。对于前两名患者,由于巨噬细胞活化综合征与转移性恶性黑色素瘤症状相似,巨噬细胞活化综合征的诊断被延迟。

讨论

转移性恶性黑色素瘤患者的巨噬细胞活化综合征诊断可能困难,因为巨噬细胞活化综合征的临床特征与转移性恶性黑色素瘤的临床特征相似。60%的巨噬细胞活化综合征患者存在高甘油三酯血症,这应促使进行骨髓穿刺检查。应系统地寻找引发感染,因为无论相关疾病是肿瘤、自身免疫性疾病,超过一半的巨噬细胞活化综合征病例都与之有关。转移性癌症患者发生的巨噬细胞活化综合征的发病机制仍未阐明。巨噬细胞活化综合征的治疗尚未达成一致,通常包括治疗相关疾病以及皮质类固醇和/或免疫抑制治疗方案。巨噬细胞活化综合征的预后通常较差,尤其是与肿瘤相关时,因为40%至60%的病例会出现致命结局。

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