Vizcaino M Adelita, Eberhart Charles G, Rodriguez Fausto J
Division of Neuropathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Department of Cellular and Tissue Biology, Faculty of Medicine, UNAM, Mexico City, Mexico.
Ocul Oncol Pathol. 2017 Dec;4(1):1-11. doi: 10.1159/000475551. Epub 2017 Jun 1.
BACKGROUND/AIMS: Hemophagocytic lymphohistiocytosis (HLH) is an infrequent inflammatory multisystemic syndrome. Only rare cases with ophthalmic involvement describing their pathologic features have been previously reported.
We report 3 cases of adult-onset HLH with bilateral ocular involvement and describe their clinicopathologic features.
Three adult males - 2 with a history of viral infection - developed persistent fever, fatigue, bone marrow abnormalities, and irreversible multiorgan failure. Visual impairment was also documented in 2 cases. Complete autopsies were performed. Ophthalmic pathology demonstrated a bilateral histiocytic infiltrate with scant lymphocytes affecting the uvea. Focal extension to the retina, optic nerve, and trabecular meshwork were also identified, as well as hemophagocytosis in 1 case. Macrophages showed strong immunoreactivity for CD163 antibody and lacked BRAF p.V600E mutant protein.
HLH is an unusual disorder associated with several systemic conditions. Histologic features in the eye are poorly documented, with prior reports restricted to children. Our 3 adult cases are reported using updated criteria and, despite the difference in age, show changes similar to those observed in the pediatric population.
背景/目的:噬血细胞性淋巴组织细胞增生症(HLH)是一种罕见的炎症性多系统综合征。此前仅有罕见的眼部受累病例报告了其病理特征。
我们报告3例成人发病的双侧眼部受累的HLH病例,并描述其临床病理特征。
3例成年男性,其中2例有病毒感染史,出现持续发热、疲劳、骨髓异常和不可逆的多器官衰竭。2例还记录有视力障碍。均进行了完整尸检。眼科病理显示双侧组织细胞浸润,淋巴细胞稀少,累及葡萄膜。还发现有局灶性扩展至视网膜、视神经和小梁网,1例有噬血细胞现象。巨噬细胞对CD163抗体呈强免疫反应性,且缺乏BRAF p.V600E突变蛋白。
HLH是一种与多种全身状况相关的罕见疾病。眼部的组织学特征记录较少,既往报告仅限于儿童。我们报告的3例成人病例采用了更新的标准,尽管年龄不同,但显示出与儿童患者相似的变化。