Uncommon histopathological features of cytomegalovirus encephalitis and measles inclusion body encephalitis on autopsy in two patients with primary immunodeficiency.

IF 0.8 4区 医学 Q4 CLINICAL NEUROLOGY Clinical Neuropathology Pub Date : 2023-01-01 DOI:10.5414/NP301476
Ankur Jindal, Deepti Suri, Kirti Gupta, Ashwani Kumar, Vignesh Pandiarajan, Rakesh Kumar Pilania, Sandesh Guleria, Amit Rawat, Sameer Vyas, Anmol Bhatia, Surjit Singh, Bishan Dass Radotra
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Abstract

Purpose: To describe the neuropathological findings in two patients with primary immunodeficiency who had fatal viral encephalitis.

Materials and methods: Severe combined immunodeficiency (SCID) was confirmed in case 1 by genetic testing, while case 2 had features suggestive of combined immunodeficiency; however, whole exome sequencing showed no pathogenic variants. Autopsies were performed in both cases after an informed consent. A detailed sampling of the brain including extracranial organs was conducted. Immunohistochemistry and electron microscopy was also performed to confirm the presence of viruses.

Results: Besides evidence of cystic encephalomalacia observed in both cases, the brain in case 1 revealed cytomegalovirus (CMV) ventriculoencephalitis accompanied by an exuberant gemistocytic response in the entire white matter. Nuclei of gemistocytes were loaded with several CMV nuclear inclusions, which was confirmed by immunohistochemistry. Case 2 demonstrated features of measles inclusion body encephalitis with several viral inclusions within neurons and astrocytes. Rare giant cells were also seen. Measles virus was confirmed on immunohistochemistry and electron microscopy. Plausibly, there was paucity of microglial nodules in both cases. Superadded bacterial pneumonia with diffuse alveolar damage was also seen in both cases.

Conclusion: These cases add to the spectrum of unusual histological features of viral encephalitis seen in patients with underlying primary immunodeficiency diseases.

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两例原发性免疫缺陷患者巨细胞病毒脑炎和麻疹包涵体脑炎尸检的不寻常组织病理学特征。
目的:描述2例原发性免疫缺陷合并致命性病毒性脑炎患者的神经病理学表现。材料与方法:病例1经基因检测确诊为重度联合免疫缺陷(SCID),病例2具有提示联合免疫缺陷的特征;然而,全外显子组测序未发现致病变异。两例均在知情同意后进行尸检。对包括颅外器官在内的大脑进行了详细的采样。免疫组织化学和电子显微镜也证实了病毒的存在。结果:除了在两例病例中观察到囊性脑软化的证据外,病例1的大脑显示巨细胞病毒(CMV)脑室脑炎,并伴有整个白质的增生细胞反应。免疫组化证实,双母细胞细胞核内携带数个巨细胞病毒核包涵体。病例2表现为麻疹包涵体脑炎的特征,在神经元和星形胶质细胞内有几个病毒包涵体。罕见的巨细胞也可见。免疫组化和电镜检查证实是麻疹病毒。很可能,这两个病例都缺乏小胶质细胞结节。两例均可见弥漫性肺泡损伤的细菌性肺炎。结论:这些病例增加了潜在原发性免疫缺陷疾病患者中病毒性脑炎的异常组织学特征。
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来源期刊
Clinical Neuropathology
Clinical Neuropathology 医学-病理学
CiteScore
1.60
自引率
0.00%
发文量
70
审稿时长
>12 weeks
期刊介绍: Clinical Neuropathology appears bi-monthly and publishes reviews and editorials, original papers, short communications and reports on recent advances in the entire field of clinical neuropathology. Papers on experimental neuropathologic subjects are accepted if they bear a close relationship to human diseases. Correspondence (letters to the editors) and current information including book announcements will also be published.
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