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儿童松果体生殖细胞瘤伴干扰素-γ受体 1 缺乏症。病例报告及文献复习。

Pineal germinoma in a child with interferon-γ receptor 1 deficiency. case report and literature review.

机构信息

Infectious Disease Department, San Martino Hospital, University of Genova, 16100, Genoa, Italy,

出版信息

J Clin Immunol. 2014 Nov;34(8):922-7. doi: 10.1007/s10875-014-0098-0. Epub 2014 Sep 14.

DOI:10.1007/s10875-014-0098-0
PMID:25216720
Abstract

Interferon-γ receptor 1 (IFN-γR1) deficiency is one of the primary immunodeficiencies conferring Mendelian Susceptibility to Mycobacterial Disease (MSMD). Some cases of neoplasms have been recently reported in patients with MSMD, underlying the already known link between immunodeficiency and carcinogenesis. We report the first case of intracranial tumour, i.e. pineal germinoma, in a 11-year-old patient with complete IFN-γR1 deficiency. The first clinical presentation of the genetic immunodeficiency dates back to when the child was aged 2 y and 10 mo, when he presented a multi-focal osteomyelitis caused by Mycobacterium scrofulaceum. The diagnosis of IFN-γR1 deficiency (523delT/523delT in IFNGR1 gene) was subsequently made. The child responded to antibiotic therapy and remained in stable clinical condition until the age of 11 years, when he started complaining of frontal, chronic headache. MRI revealed a solid pineal region mass lesion measuring 20 × 29 × 36 mm. Histological findings revealed a diagnosis of pineal germinoma. The patient received chemotherapy followed by local whole ventricular irradiation with boost on pineal site, experiencing complete remission, and to date he is tumor-free at four years follow-up. Four other cases of tumors have been reported in patients affected by MSMD in our knowledge: a case of Kaposi sarcoma, a case of B-cell lymphoma, a case of cutaneous squamous cell carcinoma and a case of oesophageal squamous cell carcinoma. In conclusion, in patients with MSMD, not only the surveillance of infectious diseases, but also that of tumors is important.

摘要

干扰素-γ 受体 1(IFN-γR1)缺陷是导致分枝杆菌病(MSMD)易感性的主要免疫缺陷之一。最近有报道称,一些 MSMD 患者发生了肿瘤,这表明免疫缺陷与致癌作用之间已经存在已知的联系。我们报告了首例颅内肿瘤,即松果体生殖细胞瘤,发生在一名 11 岁完全 IFN-γR1 缺陷患者中。该基因缺陷的首次临床表现可追溯至患儿 2 岁 10 个月时,当时他患有由耻垢分枝杆菌引起的多灶性骨髓炎。随后诊断为 IFN-γR1 缺陷(IFNGR1 基因中的 523delT/523delT)。患儿对抗生素治疗有反应,临床状况保持稳定,直到 11 岁时开始出现额部、慢性头痛。MRI 显示松果体区实性肿块病变,大小为 20×29×36mm。组织学检查显示松果体生殖细胞瘤的诊断。患者接受了化疗,随后对松果体部位进行局部全脑室照射加量,达到完全缓解,至今在 4 年随访中无肿瘤复发。据我们所知,在患有 MSMD 的患者中,已经报告了其他 4 例肿瘤病例:一例卡波西肉瘤、一例 B 细胞淋巴瘤、一例皮肤鳞状细胞癌和一例食管鳞状细胞癌。总之,在 MSMD 患者中,不仅要监测传染病,还要监测肿瘤。

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