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一名患有严重联合免疫缺陷婴儿的肠道和肺部隐孢子虫病

Intestinal and pulmonary cryptosporidiosis in an infant with severe combined immune deficiency.

作者信息

Kocoshis S A, Cibull M L, Davis T E, Hinton J T, Seip M, Banwell J G

出版信息

J Pediatr Gastroenterol Nutr. 1984;3(1):149-57. doi: 10.1097/00005176-198401000-00028.

Abstract

Small intestinal biopsy established the diagnosis of cryptosporidiosis in a 6-month-old male infant with severe combined immune deficiency. Scanning and transmission electron microscopy revealed the ultrastructural details of Cryptosporidium in several stages of development within the patient's small intestine. The organism was resistant to all antibiotics used, and the patient died in the 5th month of his illness, despite receiving parenteral alimentation and undergoing thymus transplantation. His clinical course was similar to that of other patients with fatal immune deficiencies and cryptosporidiosis. Autopsy demonstrated organisms attacking the epithelium of the small intestine, pancreatic duct, and bronchioles. Multiple organ involvement in this patient negates the view that Cryptosporidium is site-specific for a given host or is alimentary-canal-specific in humans.

摘要

小肠活检确诊一名患有严重联合免疫缺陷的6个月男婴感染了隐孢子虫病。扫描电子显微镜和透射电子显微镜揭示了患者小肠内处于几个发育阶段的隐孢子虫的超微结构细节。该病原体对所有使用的抗生素均有耐药性,尽管接受了胃肠外营养并进行了胸腺移植,该患者仍在患病第5个月死亡。他的临床病程与其他患有致命免疫缺陷和隐孢子虫病的患者相似。尸检显示病原体侵袭了小肠、胰管和细支气管的上皮。该患者多器官受累否定了隐孢子虫对特定宿主具有部位特异性或在人类中仅局限于消化道的观点。

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