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Özet: Tiroid bezinin hemanjiyomu nadir bir tanıdır ve literatürde günümüze kadar 35'ten az vaka yayınlanmıştır. Patogenezi tam bilinmemekle birlikte, anjiyoblastik mezenşimin kanal oluşturma yetersizliği ile ilişkili gelişimsel bir anomali olduğu ileri sürülmektedir. Mikroskobisinde, reaktif endotelyal hiperplazi, anjiyosarkom ve hemanjiyosarkomdan ayırt edilmelidir. Biz nonspesifik ultrasonografik görünüme sahip bir primer tiroid kavernöz hemanjiyomu olgusunu sunuyoruz. Sitolojik bulgular tanısal değildi ve kesin tanı spesimeninin patolojik incelemesinde kondu.
Summary: Thyroid gland hemangioma is a rare diagnosis and less than 35 cases have been published in literature so far. Although the pathogenesis is not fully known, it is claimed that angioblastic cystitis is a developmental anomaly associated with channeling failure. In microscopy, reactive endothelial hyperplasia, angiosarcoma and hemangiosarcoma should be distinguished. We offer a phenomenon of a primary thyroid cavernal hemangioma with an unspecific ultrasound appearance. The cytological findings were not diagnosed and the exact diagnosis was placed in the pathological examination of the specimen.
Abstract: Hemangioma of the thyroid gland is a rare diagnosis and less than 35 cases have been previously published in the literature. The pathogenesis is unknown but it is suggested to be a developmental anomaly which is associated with an incapability of angioblastic mesenchyma to form canals. On microscopic examination, it should be distinguished from reactive endothelial hyperplasia, angiosarcoma or hemangiosarcoma. We report a case of a primary thyroid hemangioma, with nonspesific US appearance. Cytologic findings were nondiagnostic and final diagnosis was made at pathologic examination of the hemithyroidectomy specimen.
Field : Sağlık Bilimleri
Journal Type : Uluslararası
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