Lanternier Fanny, Lebbé Céleste, Schartz Noël, Farhi David, Marcelin Anne-Geneviève, Kérob Delphine, Agbalika Félix, Vérola Olivier, Gorin Isabelle, Janier Michel, Avril Marie-Françoise, Dupin Nicolas
Department of Dermatology, Cochin Hospital, APHP, Faculté de Médecine René Descartes, Paris, France.
AIDS. 2008 Jun 19;22(10):1163-8. doi: 10.1097/QAD.0b013e3283031a8a.
Four epidemiologic forms of Kaposi's sarcoma have been described, all of which are associated with the human herpesvirus-8. In western countries, human herpesvirus-8 is more prevalent in homosexual men than in the general population, and anecdotal cases of Kaposi's sarcoma in HIV-negative homosexual men have been reported.
We included HIV-negative homosexual and bisexual male patients with histologically proven Kaposi's sarcoma in a retrospective study. Clinical data were collected using a standardized form. Risk factors for human herpesvirus-8 infection and for the development of Kaposi's sarcoma were systematically recorded.
Between 1995 and 2007, 28 men met the defined inclusion criteria. Mean age at first symptoms of Kaposi's sarcoma was 53 years. Clinical presentation resembled classical Kaposi's sarcoma, with limited disease in most patients. No cellular or humoral immunodeficiency was observed. Serologic tests for human herpesvirus-8 (latent immunofluorescence assay) were positive in 88% of patients, and only two patients displayed human herpesvirus-8 viremia at the time of Kaposi's sarcoma diagnosis. Three patients developed lymphoproliferative disorders (Castleman disease, follicular lymphoma and Burkitt lymphoma). In this population, alpha-interferon was well tolerated and gave a complete response, but most patients require only local treatment, if any.
Kaposi's sarcoma may develop in homosexual or bisexual men without HIV infection. This type of Kaposi's sarcoma has clinical features in common with classical Kaposi's sarcoma but occurs in younger patients. Its prognosis is good, as Kaposi's sarcoma is generally limited, but clinicians should be aware of the association with lymphoproliferative diseases, which may affect prognosis.
已描述了卡波西肉瘤的四种流行病学形式,所有这些形式均与人类疱疹病毒8型相关。在西方国家,人类疱疹病毒8型在男同性恋者中比在普通人群中更普遍,并且已有关于HIV阴性男同性恋者患卡波西肉瘤的个别病例报道。
我们纳入了经组织学证实患有卡波西肉瘤的HIV阴性男同性恋和双性恋男性患者进行一项回顾性研究。使用标准化表格收集临床数据。系统记录人类疱疹病毒8型感染和卡波西肉瘤发生的危险因素。
在1995年至2007年期间,28名男性符合确定的纳入标准。卡波西肉瘤首次出现症状时的平均年龄为53岁。临床表现类似于经典卡波西肉瘤,大多数患者疾病局限。未观察到细胞或体液免疫缺陷。88%的患者人类疱疹病毒8型血清学检测(潜在免疫荧光测定)呈阳性,并且在卡波西肉瘤诊断时只有两名患者出现人类疱疹病毒8型病毒血症。三名患者发生了淋巴增殖性疾病(卡斯特曼病、滤泡性淋巴瘤和伯基特淋巴瘤)。在该人群中,α干扰素耐受性良好并产生了完全缓解,但大多数患者仅需局部治疗(如果需要治疗的话)。
卡波西肉瘤可能在未感染HIV的男同性恋或双性恋男性中发生。这种类型的卡波西肉瘤与经典卡波西肉瘤具有共同的临床特征,但发生于较年轻的患者。其预后良好,因为卡波西肉瘤通常局限,但临床医生应注意其与可能影响预后的淋巴增殖性疾病的关联。