Mahajan Vikram K, Raina Rashmi Kaul, Singh Suman, Rashpa Rattan Sagar, Sood Anuradha, Chauhan Pushpinder S, Mehta Karaninder S, Rawat Ritu, Sharma Vikas
Department of Dermatology, Venereology and Leprosy, Dr. R. P. Govt. Medical College, Kangra (Tanda), Himachal Pradesh, India.
Department of Pathology, Dr. R. P. Govt. Medical College, Kangra (Tanda), Himachal Pradesh, India.
Am J Trop Med Hyg. 2017 Dec;97(6):1749-1756. doi: 10.4269/ajtmh.17-0432. Epub 2017 Sep 21.
We describe four cases of histoplasmosis indigenous to Himachal Pradesh (India) that will be of considerable public health interest. A 48-year-old human immunodeficiency virus (HIV)-negative man with cervical and mediastinal lymphadenopathy, hepatosplenomegaly, adrenal mass, and bone marrow involvement was treated as disseminated tuberculosis without benefit. Progressive disseminated histoplasmosis was diagnosed from the fungus in smears from adrenal mass. Another 37-year-old HIV-positive man was on treatment of suspected pulmonary tuberculosis. He developed numerous erythema nodosum leprosum-like mucocutanous lesions accompanied by fever, generalized lymphadenopathy, and weight loss. Pulmonary histoplasmosis with cutaneous dissemination was diagnosed when skin lesions showed the fungus in smears, histopathology, and mycologic culture. Both were successfully treated with amphotericin B/itraconazole. Third patient, a 46-year-old HIV-negative man, had oropharyngeal lesions, cervical lymphadenopathy, intermittent fever, hepatosplenomegaly, and deteriorating general health. Progressive disseminated oropharyngeal histoplasmosis was diagnosed from the fungus in smears and mycologic cultures from oropharyngeal lesions and cervical lymph node aspirates. He died despite initiating treatment with oral itraconazole. Another 32-year-old man 3 months after roadside trauma developed a large ulcer with exuberant granulation tissue over left thigh without evidence of immunosuppression/systemic involvement. He was treated successfully with surgical excision of ulcer under amphotericin B/itraconazole coverage as primary cutaneous histoplasmosis confirmed pathologically and mycologically. A clinical suspicion remains paramount for early diagnosis of histoplasmosis particularly in a nonendemic area. Most importantly, with such diverse clinical presentation and therapeutic outcome selection of an appropriate and customized treatment schedule is a discretion the treating clinicians need to make.
我们描述了印度喜马偕尔邦本土发生的4例组织胞浆菌病病例,这些病例具有重大的公共卫生意义。一名48岁的人类免疫缺陷病毒(HIV)阴性男性,患有颈部和纵隔淋巴结病、肝脾肿大、肾上腺肿块以及骨髓受累,曾被当作播散性结核病治疗但未见好转。从肾上腺肿块涂片的真菌中诊断出进行性播散性组织胞浆菌病。另一名37岁的HIV阳性男性正在接受疑似肺结核的治疗。他出现了许多类麻风结节性红斑样皮肤黏膜病变,并伴有发热、全身淋巴结病和体重减轻。当皮肤病变在涂片、组织病理学和真菌培养中显示出真菌时,诊断为伴有皮肤播散的肺组织胞浆菌病。两人均用两性霉素B/伊曲康唑成功治疗。第三名患者是一名46岁的HIV阴性男性,有口咽病变、颈部淋巴结病、间歇性发热、肝脾肿大,全身健康状况不断恶化。从口咽病变和颈部淋巴结穿刺物的涂片及真菌培养中的真菌诊断出进行性播散性口咽组织胞浆菌病。尽管开始用口服伊曲康唑治疗,他仍死亡。另一名32岁男性在路边创伤3个月后,左大腿出现一个有大量肉芽组织的大溃疡,无免疫抑制/全身受累迹象。经病理和真菌学确诊为原发性皮肤组织胞浆菌病,在两性霉素B/伊曲康唑覆盖下手术切除溃疡,治疗成功。对于组织胞浆菌病的早期诊断,临床怀疑仍然至关重要,尤其是在非流行地区。最重要的是,鉴于临床表现如此多样以及治疗结果各异,选择合适且定制化的治疗方案是主治临床医生需要做出的决定。