Coexistence of monomorphic epitheliotropic intestinal T-cell lymphoma of the jejunum and bilateral adrenal pheochromocytomas: A case report.

Tamaki Ichikawa, Makiko Kobayashi, Shunro Matsumoto, Rikio Suzuki, Sakura Tomita, Naoya Nakamura, Jun Hashimoto

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In one paragraph

Article in Radiology case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed

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5 · Who and what money

Authors and funding

7 authors.

Tamaki IchikawaDepartment of Radiology, Tokai University School of Medicine, Isehara, Kanagawa, Japan.

Makiko KobayashiDepartment of Radiology, Tokai University School of Medicine, Isehara, Kanagawa, Japan.

Shunro MatsumotoDepartment of Radiology, Oita City Medical Association's Almeida Hospital, Isehara, Kanagawa, Japan.

Rikio SuzukiDepartment of Hematology/oncology, Tokai University School of Medicine, Isehara, Kanagawa, Japan.

Sakura TomitaDepartment of Pathology, Tokai University School of Medicine, Isehara, Kanagawa, Japan.

Naoya NakamuraDepartment of Pathology, Tokai University School of Medicine, Isehara, Kanagawa, Japan.

Jun HashimotoDepartment of Radiology, Tokai University School of Medicine, Isehara, Kanagawa, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Monomorphic epitheliotropic intestinal T-cell lymphoma (MEITL) is rare and aggressive form of intestinal lymphoma. We report a 52-year-old man with coexisting MEITL of the jejunum and bilateral adrenal pheochromocytomas. PET-CT revealed a small jejunal mass with intestinal wall thickening (SUVmax: 21) and bilateral adrenal lesions (SUVmax: 10). Diffusion-weighted whole-body imaging with background body signal suppression (DWIBS) showed restricted diffusion in the jejunal mass [Apparent diffusion coefficient (ADC): 0.71 × 10

Indexed as

Monomorphic epitheliotropic intestinal T-cell lymphomaPET-CTPheochromocytomas

Identifiers

PMID41328359

DOI10.1016/j.radcr.2025.09.021

PMCPMC12664797

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