RESUMO
Cavernous hemangiomas are unusual tumors with a propensity for skin and liver involvement and rarely involving adrenal gland.Adrenal hemangiomas are nonfunctioning tumors, usually discovered at autopsy. In 1955, Johnson and Jeppensen reported the first adrenal hemangioma to be removed surgically.One case of emangioma of the adrenal gland was reported in Korea. We report a case of a cavernous hemangioma of the adrenal gland which was successfully treated surgically.In addition, we review the clinical, radiographic, and pathologic features of this disease. With the advance of diagnostic thchniques in arterography, ultrasound, and computerized tomography, preoperative recognition and diagnosis should be simplified and surgical removal carried out to rule out possible malignancy, preclude traumatic rupture, or relieve symptoms of the mass.
Assuntos
Glândulas Suprarrenais , Autopsia , Diagnóstico , Hemangioma , Hemangioma Cavernoso , Coreia (Geográfico) , Fígado , Ruptura , Pele , UltrassonografiaRESUMO
Leiomyosarcomas make up approximately 1 to 3% of all gastric neoplasms. The most prevalent age group was 6th and 7th decades. The main symptoms and signs were abdominal pain and bleeding. They most frequently involve gastric body and often ulcerate and bleed. Diagnosis can be established only by exploratory operation and histologic examination. Leiomyosarcomas rarely invade adjacent viscera and characteristically do not metastasize to lymph nodes, but they may spread to the liver and lungs. The treatment of choice is surgical resection. We report two cases of gastric leiomyosarcoma which was successfully treated surgically.
Assuntos
Humanos , Dor Abdominal , Diagnóstico , Hemorragia , Leiomiossarcoma , Fígado , Pulmão , Linfonodos , Neoplasias Gástricas , Estômago , Úlcera , VíscerasRESUMO
Hepatoma is one of the most common malignant disease among cancers that occur in Korea. Recently, according ta developing imaging diagnostic technology and non surgical treatment the hepatoma is easily detected in early diagnosis and appropriate treatment. From this point of view, the histologic pattern of hepatoma is markedly important. This is the first reported case of sclerosing hepatocellular carcinoma, which is characterized by intense fibrosis, in which the tubular neoplastic structures are embedded. The incidence of sclerosing hepatocellular carcinoma is very rare. Therefore the rare histologic pattern of hepatoma might be introduced by many studies and reports. We recently experienced a case of sclerosing hepatocellular carcinoma.