15 November 2020>: Articles
Langerhans Cell Histiocytosis with Uncommon Liver Involvement: A Case Report
Challenging differential diagnosis, Rare disease
Alfonso Reginelli A* , Maria Pignatiello E , Fabrizio Urraro B , Maria Paola Belfiore A , Giorgio Toni B , Giovanna Vacca A , Salvatore Cappabianca FDOI: 10.12659/AJCR.923505
Am J Case Rep 2020; 21:e923505
Figure 5. (A) Hepatic core needle biopsy: Hematoxylin/eosin-stained slides show hepatic parenchyma almost completely substituted by a middle-size cell population characterized by nuclei with membrane irregularity, with incision, dispersed chromatin, and slightly eosinophilic cytoplasm. A mixed infiltrate composed of lymphocytes, plasma cells, histiocytes, and numerous eosinophil granulocytes were also present around the lesions. There was moderate fibrosis, with disappearance of the portal spaces. (B) Immunohistochemistry showed positivity for CD1a.