Littoral Cell Angioma of the Spleen: An Additional Report of Four Cases with Emphasis on the Association with Visceral Organ Cancers

Author:

Bisceglia Michele1,Sickel Joshua Z.2,Giangaspero Felice3,Gomes Vito4,Amini Mostafà4,Michal Michal5

Affiliation:

1. Servizio di Anatomia Patologica, IRCCS-Ospedale “Casa Sollievo della Sofferenza”, San Giovanni Rotondo, Italy

2. Pathology Department, El Camino Hospital, Mountain View, California, USA

3. Servizio di Anatomia Patologica, Ospedale “M. Bufalini”, Cesena

4. Servizio di Anatomia Patologica, Ospedale Grande degli Infermi, Viterbo, Italy

5. Department of Pathology, Charles University Medical Faculty, Pilsen, Czech Republic Viterbo, Italy

Abstract

Aims and background Littoral cell angioma (LCA) is an uncommon vascular tumor of the spleen recently described and interpreted as the tumoral counterpart of the normally present littoral cells lining the splenic sinus channels of red pulp. The diagnosis of LCA is suggested by a quite characteristic morphology and confirmed by the demonstration of a hybrid endothelial/histiocytic phenotype. Methods Four original and previously unreported cases of LCA are presented. All four splenic vascular tumors were investigated by light microscopy and immunohistochemistry for endothelial and histiocytic markers. Results All four cases were associated with visceral epithelial malignancies (colorectal adenocarcinoma in two cases, renal and pancreatic adenocarcinoma in one case each). One case was also associated with an intracranial tentorial meningioma. Conclusions We consider our findings as a novelty and signal the possible existence of a clinical syndrome. Five of a total of 21 previously reported cases in the literature were also described as being associated with other cancers (non-Hodgkin's lymphoma in two cases, two not further specified tumors of the liver and brain, an epithelial ovarian cancer, and a non-small cell lung cancer in one case each). Close follow-up and careful investigation in search of a second visceral neoplasm are strongly recommended in cases of LCA, but further clinical observations and more in-depth genetic and molecular studies are needed before any valid conclusions can be drawn.

Publisher

SAGE Publications

Subject

Cancer Research,Oncology,General Medicine

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