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[脊髓组织胞浆菌病。病例报告]

[Spinal cord histoplasmoma. A case report].

作者信息

Rivierez M, Heyman D, Brebion A, Landau-Ossondo M, Desbois N, Vally P

机构信息

Service de Neurochirurgie, Hospital P. Zobda-Quitman, CHU, 97200 Fort-de-France.

出版信息

Neurochirurgie. 2002 Feb;48(1):44-8.

Abstract

Over a period of 2 months, a 60-year-old man, a chicken breeder, experienced low back pain, lower limb weakness predominant on the right side, and urinary difficulties, leading progressively to a flaccid paraplegia with sphincter impairment. Concomitant poor cognitive performances were noted. MRI showed enlargement of the conus terminalis, with a low-intensity signal on T1-weighted images, high-intensity signal on T2-weighted images, and areas of intramedullar contrast enhancement. A biopsy of the lesion showed macrophages containing yeast cells, with PAS and Grocott staining aspects compatible with the presence of Histoplasma capsulatum (Hc). A brain MRI showed multiple localizations in the brain stem and in both hemispheres with associated edema. Disseminated histoplasmosis was confirmed by a biopsy of a sub-maxillary ganglion demonstrating a necrotic tuberculoid lymphadenitis containing yeast cells resembling Hc. Immune tests disclosed the presence of HTLV1 anti-bodies without immunodeficiency nor HIV co-infection. An anti-micotic treatment was started 2 weeks after surgery, with intra-venous amphotericin B, for 21 days, followed by itraconazole, orally for 90 days. Cognitive functions improved significantly in 5 weeks while paraplegia and sphincter impairment remained unchanged. Seven months later, cerebral MR aspects dramatically improved while the conus medullaris lesion diminished, and the edematous component disappeared in all areas. Even though histoplasmosis is endemic in our region, CNS localization is rare, generally in disseminated forms associated with immunodeficiency. Brain granulomas are well-known, but spinal cord histoplasmomas are exceptional: only four cases have been evaluated by MRI. Unlike our case, spinal cord forms generally improve, due to surgery associated with antifungus medication, or sometimes due to specific medical treatment alone but with sufficient dosage.

摘要

在两个月的时间里,一名60岁的男性养鸡户出现了腰痛、以下肢右侧为主的下肢无力和排尿困难,逐渐发展为弛缓性截瘫并伴有括约肌功能障碍。同时还发现其认知功能较差。磁共振成像(MRI)显示终丝增粗,在T1加权图像上呈低信号,在T2加权图像上呈高信号,髓内有强化区域。病变活检显示巨噬细胞内含有酵母细胞,过碘酸雪夫(PAS)染色和格罗科特(Grocott)染色结果与荚膜组织胞浆菌(Hc)相符。脑部MRI显示脑干和双侧大脑半球有多处病灶并伴有水肿。通过对颌下神经节活检证实为播散性组织胞浆菌病,显示为坏死性结核样淋巴结炎,含有类似Hc的酵母细胞。免疫检测发现存在人类嗜T淋巴细胞病毒1型(HTLV1)抗体,无免疫缺陷,也未合并人类免疫缺陷病毒(HIV)感染。术后两周开始抗真菌治疗,静脉注射两性霉素B,持续21天,随后口服伊曲康唑90天。5周时认知功能显著改善,而截瘫和括约肌功能障碍仍无变化。7个月后,脑部MRI表现显著改善,脊髓圆锥病变缩小,所有区域的水肿成分均消失。尽管组织胞浆菌病在我们地区为地方病,但中枢神经系统定位罕见,通常以与免疫缺陷相关的播散形式出现。脑肉芽肿是众所周知的,但脊髓组织胞浆瘤则很罕见:仅有4例通过MRI评估。与我们的病例不同,脊髓型组织胞浆菌病通常会改善,这得益于手术联合抗真菌药物治疗,或者有时仅通过足够剂量的特定药物治疗。

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