Intravascular lymphoma with hypopituitarism: A case report

doi:10.5306/wjco.v11.i8.673

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World Journal of Clinical Oncology

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2218-4333

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

Case Report

World J Clin Oncol. Aug 24, 2020; 11(8): 673-678
Published online Aug 24, 2020. doi: 10.5306/wjco.v11.i8.673

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Figure 1 Magnetic resonance imaging: T1-weighted imaging. A and B: At presentation: coronary (A) and sagittal (B) view magnetic resonance images (MRI) showing an enlarged pituitary gland; C and D: Three months later (after the third cycle of chemotherapy): Coronary (C) and sagittal (D) view MRI showing substantial mass reduction.

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Figure 2 Bone marrow aspiration showing hemophagocytosis (designated by an arrow). A and B: Wright and Giemsa staining at ×400 (A) and ×1000 (B) magnification.

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Figure 3 Hematoxylin and eosin. A and B: Histopathology of intravascular lymphoma by random skin biopsy: the arrows indicate lymphoma cells seen within the lumen of small vessels: hematoxylin and eosin stain at ×400 (A) and ×1000 (B) magnification.

Citation: Kawahigashi T, Teshima S, Tanaka E. Intravascular lymphoma with hypopituitarism: A case report. World J Clin Oncol 2020; 11(8): 673-678
URL: https://www.wjgnet.com/2218-4333/full/v11/i8/673.htm
DOI: https://dx.doi.org/10.5306/wjco.v11.i8.673