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Medicine · 2026

Pulmonary adenofibroma: MSCT and clinicopathological analysis of three case reports and a literature review.

СтатьяКлинический случайОбзорНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
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Chen Wang, Liu Kang, Zhao Yang, Liu Chen-Chen, Cao Meng-Yu, Wang Xiao-Juan

Аннотация

RATIONALE: Pulmonary adenofibroma (PAF) is a rare, benign lung tumor, classified as a primary fibroepithelial tumor of the lung.

PATIENT CONCERNS: This study reports 3 cases of pulmonary adenofibroma (PAF). Case 1 was a solitary tumor presenting with a cough; Case 2 was a solitary tumor manifesting as chest tightness and pain; Case 3 was a multiple-lesion variant in an asymptomatic patient.

DIAGNOSES: Pulmonary lesions were detected in all patients by computed tomography (CT) and were ultimately diagnosed as PAF through histopathological analysis.

INTERVENTIONS: Cases 1 and 2 underwent video-assisted thoracoscopic wedge resection, while Case 3 received conservative management with active surveillance.

OUTCOMES: Cases 1 and 2 recovered well postoperatively, with no signs of recurrence or metastasis during follow-up. Case 3 remained stable, with some nodules demonstrating slow growth and no evidence of metastasis.

LESSONS: Pulmonary adenofibroma is readily confused with hamartoma and solitary fibrous tumor, and definitive diagnosis relies on histopathological examination.The tumor demonstrates indolent biological behavior and a favorable prognosis; therefore, overtreatment should be avoided in clinical practice.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты