The patient underwent left radical adrenalectomy after the hormonal evaluation of the tumor due to the high probability of adrenocortical carcinoma. Magnetic resonance imaging of the retroperitoneal space showed a heterogeneously enhanced mass, measuring 10x8.2 cm, with characteristics suspicious of malignancy. We report the case of a 62-year-old male with an incidentally found left adrenal mass. The tumour type but also for predicting the biologicalĪdrenal leiomyosarcomas are rare mesenchymal tumors of the suprarenal region that are usually diagnosed after they have reached a large size. Its diagnosis is based entirely on theįindings of both histological and immunohistochemical (IHC) evaluations, which are indispensable not only for determining That diagnosis of the disease is delayed because mostĬlinicians would not be familiar with its presentation, diagnosisĪnd management. Pathological characteristics, along with its rarity of chest wallīecause this entity is rarely encountered, there is the possibility Primary adrenal leiomyosarcoma and review the clinical and In the present case, we report another case of It has been reported only in 35 patients in the English Leiomyosarcoma of the adrenal gland is most
The smooth muscle wall of the central adrenal vein and itsīranches. Primary adrenal leiomyosarcoma (PAL) isĪn extremely rare mesenchymal tumour and originates from Tumours are even rarer and include angiosarcoma and
Mesenchymal tumours of adrenal gland are rare.
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