ArticleClinical case reports2022
Collision lung tumor associating typical carcinoid tumor to sclerosing hemangioma.
Article in Clinical case reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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Who cites it
6 citing papers in PubMed, 4 citations in OpenAlex.
- Pulmonary Collision Tumor Comprising Lung Adenocarcinoma and Metastatic Endometrial Cancer: A Case Report.Thoracic cancer · 2026Article
- Sclerosing pneumocytoma mixed with a typical carcinoid: a case report and review of literature.International journal of surgery case reports · 2026Article
- Article
- Revisiting Pulmonary Sclerosing Pneumocytoma.Clinics and practice · 2024Review
- Giant pulmonary sclerosing pneumocytoma with potentially malignant biological behavior: a case report and literature review.Annals of translational medicine · 2023Article
- Collision lung tumor associating typical carcinoid tumor to sclerosing hemangioma.Clinical case reports · 2022Article
Corrections and comments
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Authors and funding
7 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Collision tumors associating carcinoid tumor and sclerosing pneumocytoma have rarely been reported in the literature. The clinical presentation may be challenging especially in cases showing multiple and bilateral nodules. This case illustrates the association of both tumors diagnosed incidentally and illustrates a full spectrum of neuroendocrine lesions and sclerosing pneumocytoma. The authors present the case of a 52-year-old patient presenting an abdominal pain revealing a vesicular lithiasis and multiple pulmonary nodules. Radiologic follow-up of the asymptomatic lung lesions revealed the stabilization of a left lobe lesion with a disappearance of the other lesions. A lobectomy with a mediastinal lymph node curettage was performed. The microscopic examination revealed both tumor components associating a typical carcinoid tumor to a sclerosing pneumocytoma in association to lesions of diffuse neuroendocrine hyperplasia present in the peri-tumoral parenchyma. This case illustrates radiologic, gross, and microscopic features of a rare pulmonary tumor.
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Registered trials
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