Splenic Hamartoma: Immunohistochemical and Ultrastructural Profile of Two Cases

Author:

Ali Tehmina Z.,Beyer Ginine1,Taylor Michelle,Volpe Carmine2,Papadimitriou John C.3

Affiliation:

1. Department of Pathology, University of Maryland Medical Center, Baltimore, Maryland.

2. Surgery, University of Maryland Medical Center, Baltimore, Maryland.

3. University of Maryland Medical Center, Department of Pathology, 22 S. Greene Street, Baltimore MD 21201.

Abstract

Splenic hamartoma (SH) is a rare, benign lesion. We present 2 cases, both in females (2 and 30 years, respectively) with multiple urinary tract infections, and left upper quadrant abdominal pain. Immunohistochemical staining with factor VIII displayed intense diffuse staining in the SH with corresponding weak staining in the adjacent spleen. CD31 showed a reverse pattern from that of factor VIII. CD34 staining pattern was identical in both the spleen and the SH. Ultrastructurally, the SH showed endothelial cells with relatively empty cytoplasm, scattered Weibel Palade bodies, and lining by basement membrane surrounded by fibrous long-spacing collagen. Our study highlights the unique immunohistochemical profile of SH. The ultrastructural features are interesting, although their diagnostic significance remains to be confirmed in future studies.

Publisher

SAGE Publications

Subject

Pathology and Forensic Medicine,Surgery,Anatomy

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1. Segment-Long-Spacing (SLS) and the Polymorphic Structures of Fibrillar Collagen;Subcellular Biochemistry;2022

2. A splenic hamartoma: Adding a new case to the literature: A case report;International Journal of Surgery Case Reports;2022-01

3. Hamartoma of the Spleen and Lymph Nodes;Encyclopedia of Pathology;2019-10-31

4. Hamartoma of the Spleen and Lymph Nodes;Encyclopedia of Pathology;2019

5. A giant splenic hamartoma associated with hematologic disorders: A case report;Annals of Medicine and Surgery;2018-12

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