Advanced age chest wall hamartoma and typical carcinoid tumor: a very rare coexistence
Rasih Yazkan1,Muhammed Samet Ozdemir1,Suleyman Emre Akın1,Hasan Ekrem Camas1,Özgecan Afacan2
Current Thoracic Surgery
2025;10(1):025-028.
1Department of Thoracic Surgery, Faculty of Medicine, Suleyman Demirel University, Isparta, Turkey
2Department of Thoracic Pathology, Faculty of Medicine, Suleyman Demirel University, Isparta, Turkey
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Chest wall hamartoma is a rare pathology in adults, usually presenting at birth or in early infancy. They may
present with compression symptoms depending on their localization. Although it is rare to be recognized
with late-onset symptoms in adults, it requires differential diagnosis with other malignant and benign
tumors of the chest wall. Histologically, carcinoid tumors are classified into two subgroups as typical
and atypical. Atypical carcinoids have an aggressive course and have the potential for metastasis and
recurrence. Typical carcinoids are low grade malignancies. Although the prognosis of carcinoid tumors
after surgical resection is reported to be good, a variable prognosis has been reported. The size of the tumor,
histological type, nodal involvement, and distant metastasis are thought to affect the prognosis. Herein we
present an elderly patient with chest wall hamartoma and typical carcinoid, in the light of literature.
Keywords :
chest wall, carcinoid tumor, hamartoma