ArticleRomanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie
The clinicopathological challenges of symptomatic and incidental pulmonary hamartomas diagnosis.
Article in Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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10 citing papers in PubMed, 13 citations in OpenAlex.
- Predictive Value of Semi-Quantitative GeneXpert Categories for Microbiological Outcomes in Pulmonary Tuberculosis.Biomedicines · 2026Article
- Incidentally Discovered Pulmonary Hamartoma: A Case Report and Review of the Literature.Cureus · 2026Article
- Pulmonary Adenoleiomyomatous Hamartoma: Case Report of a Rare Entity With Comprehensive Literature Review.Case reports in pathology · 2026Article
- Endobronchial hamartoma; are the lines fading from the zebra? Case series and review of literature.Lung India : official organ of Indian Chest Society · 2025Article
- Endobronchial hamartomas as a rare cause of chronic cough.Respiratory medicine case reports · 2025Article
- Pediatric solitary pulmonary tuberculoma mimicking peripheral pulmonary hamartoma with extensive pleural adhesions: a case report.Frontiers in medicine · 2025Article
- The diagnostic value of CT-guided percutaneous lung biopsy in atypical pulmonary hamartoma and pulmonary sclerosing pneumocytoma.Frontiers in oncology · 2025Article
- A rare case of asymptomatic giant pulmonary hamartoma.Diagnostic pathology · 2024Article
- Case Report: Giant lung hamartoma : An usual cause of lobectomy in a five-year child.F1000Research · 2024Article
- Posterior urethral hamartoma with hypospadias in a child: a case report and literature review.Frontiers in pediatrics · 2023Article
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8 authors at 2 institutions in 1 country.
Funding
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Abstract
Pulmonary hamartomas (PHs) are the most common benign lung tumors. Usually, they are asymptomatic and incidentally discovered during assessment for other diseases or during the autopsy exam. In this context, we have performed a retrospective analysis of surgical resections in a 5-year series of patients diagnosed with PHs in the Clinic of Pulmonary Diseases, Iaşi, Romania, aiming to evaluate their clinicopathological features. A total of 27 patients with PH (40.74% males and 59.26% females) were evaluated. 33.33% of patients were asymptomatic, while the others exhibited variable symptoms, such as chronic cough, dyspnea, chest pain or weight loss. In most cases, PHs presented as solitary nodules, predominantly disposed in the right upper lobe (40.74% of cases), followed by the right lower lobe (33.34%), and left lower lobe (18.51%). The microscopic examination revealed a mixture of mature mesenchymal tissue, such as hyaline cartilage, adipose tissue, fibromyxoid tissue, and smooth muscle bundles, in variable proportions, associated with clefts of entrapped benign epithelium. A dominant adipose tissue component was observed in one case. PH was associated with a history of extrapulmonary cancer diagnosis, in one patient. Although considered benign lung tumors, PHs diagnosis and therapy may be challenging. Having in mind the possibility of recurrence or their occurrence as a part of specific syndromes, PHs should be thoroughly investigated for an appropriate patients' management. Their complex significance and the correlation with other types of lesions, including malignancies, may be further studied, by more extensive studies of surgical and necroptic cases.
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