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ArticleRespiratory medicine case reports2025

Lymphangiomatosis diagnosed using transbronchial lung cryobiopsy: A case report.

Ken Ito, Naoyuki Kuse, Akari Misumi, Maeda Takashi, Haruka Chin, Yu Ito, Shuya Miyazaki, Keita Sakamoto, Nobuyasu Awano, Minoru Inomata and 4 more

Abstract readCase Reports
In one paragraph

Article in Respiratory medicine case reports, 2025. 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

14 authors.

Ken ItoDepartment of Respiratory Medicine, Japanese Red Cross Medical Center, Japan.
Naoyuki KuseDepartment of Respiratory Medicine, Japanese Red Cross Medical Center, Japan.
Akari MisumiDepartment of Respiratory Medicine, Japanese Red Cross Medical Center, Japan.
Maeda TakashiDepartment of Respiratory Medicine, Japanese Red Cross Medical Center, Japan.
Haruka ChinDepartment of Respiratory Medicine, Japanese Red Cross Medical Center, Japan.
Yu ItoDepartment of Respiratory Medicine, Japanese Red Cross Medical Center, Japan.
Shuya MiyazakiDepartment of Respiratory Medicine, Japanese Red Cross Medical Center, Japan.
Keita SakamotoDepartment of Respiratory Medicine, Japanese Red Cross Medical Center, Japan.
Nobuyasu AwanoDepartment of Respiratory Medicine, Japanese Red Cross Medical Center, Japan.
Minoru InomataDepartment of Respiratory Medicine, Japanese Red Cross Medical Center, Japan.
Yuki KobayashiDepartment of Pathology Medicine, Japanese Red Cross Medical Center, Japan.
Toshio KumasakaDepartment of Pathology Medicine, Japanese Red Cross Medical Center, Japan.
Yuan BaeDepartment of Pathology Medicine, Japanese Red Cross Medical Center, Japan.
Takehiro IzumoDepartment of Respiratory Medicine, Japanese Red Cross Medical Center, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lymphangiomatosis, a rare systemic condition characterized by abnormally dilated lymphatic structures affecting multiple organs, is typically diagnosed using surgical lung biopsy or lymphangiography, both of which present significant technical challenges. Here, we report the first case of lymphangiomatosis diagnosed using transbronchial lung cryobiopsy (TBLC) in a 20-year-old asymptomatic man. The medical history of the patient was unremarkable, and chest computed tomography revealed diffuse interstitial thickening, ground-glass opacities, and pericardial effusion. Abdominal imaging indicated multiple low-attenuation nodules in the mesentery, omentum, and retroperitoneal areas. Positron emission tomography-computed tomography revealed no abnormal fluorodeoxyglucose uptake in any lesion. TBLC specimens had irregularly dilated lymphatics in the interlobular septa and around vascular bundles, as well as peripheral alveolar walls showing lymphatic dilations positive for D2-40, confirming lymphangiomatosis. The patient was asymptomatic, and careful follow-up was initiated without treatment. This case demonstrates that TBLC may serve as an effective, minimally invasive diagnostic tool for lymphangiomatosis. Early diagnosis during the asymptomatic phase may be crucial given the potential for severe complications associated with thoracic involvement.

Indexed as

LymphangiomatosisTBLCTransbronchial lung cryobiopsy

Identifiers

PMID40502211
PMCPMC12152360

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