Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 4 de 4
Filtrar
1.
Journal of Korean Society of Endocrinology ; : 268-272, 2005.
Artículo en Coreano | WPRIM | ID: wpr-141533

RESUMEN

A primary thyroid lymphoma is rare among all types of thyroid malignancy. Usually, a thyroid lymphoma is associated with underlying chronic autoimmune thyroiditis. Recently, we experienced a primary thyroid mucosa-associated lymphoid tissue(MALT) lymphoma, with an incidental micropapillary thyroid carcinoma, but lacking evidence of autoimmune thyroiditis. A female patient visited our hospital for further evaluation of a rapidly enlarging, painless thyroid mass which had been stable for 8 years. Lymphocytic thyroiditis or a lymphoma was suspected from fine needle aspiration performed at another hospital. The thyroid function test and other routine laboratory tests were normal. The histopathological findings after a total thyroidectomy revealed a MALT lymphoma with a micropapillary thyroid carcinoma. There was no evidence of chronic autoimmune thyroiditis. This is, to the best of our knowledge, the first case report of a MALT lymphoma arising from the thyroid gland without evidence of chronic autoimmune thyroiditis in Korea


Asunto(s)
Femenino , Humanos , Biopsia con Aguja Fina , Corea (Geográfico) , Linfoma , Linfoma de Células B de la Zona Marginal , Pruebas de Función de la Tiroides , Glándula Tiroides , Neoplasias de la Tiroides , Tiroidectomía , Tiroiditis Autoinmune
2.
Journal of Korean Society of Endocrinology ; : 268-272, 2005.
Artículo en Coreano | WPRIM | ID: wpr-141532

RESUMEN

A primary thyroid lymphoma is rare among all types of thyroid malignancy. Usually, a thyroid lymphoma is associated with underlying chronic autoimmune thyroiditis. Recently, we experienced a primary thyroid mucosa-associated lymphoid tissue(MALT) lymphoma, with an incidental micropapillary thyroid carcinoma, but lacking evidence of autoimmune thyroiditis. A female patient visited our hospital for further evaluation of a rapidly enlarging, painless thyroid mass which had been stable for 8 years. Lymphocytic thyroiditis or a lymphoma was suspected from fine needle aspiration performed at another hospital. The thyroid function test and other routine laboratory tests were normal. The histopathological findings after a total thyroidectomy revealed a MALT lymphoma with a micropapillary thyroid carcinoma. There was no evidence of chronic autoimmune thyroiditis. This is, to the best of our knowledge, the first case report of a MALT lymphoma arising from the thyroid gland without evidence of chronic autoimmune thyroiditis in Korea


Asunto(s)
Femenino , Humanos , Biopsia con Aguja Fina , Corea (Geográfico) , Linfoma , Linfoma de Células B de la Zona Marginal , Pruebas de Función de la Tiroides , Glándula Tiroides , Neoplasias de la Tiroides , Tiroidectomía , Tiroiditis Autoinmune
3.
Korean Journal of Gastrointestinal Endoscopy ; : 534-538, 2004.
Artículo en Coreano | WPRIM | ID: wpr-92190

RESUMEN

Endometriosis is the abnormal growth of endometrial tissue outside of uterine cavity. The incidence of endometriosis is estimated about 8~15% of the reproductive women. The intestinal invasion is showed at about 3~34%. The intestinal invasion may be involved in rectosigmoid colon, appedix, ileum, and cecum in order of decreasing frequency. Until now, only 7 cases have been reported in Korea. Most cases are diagnosed after surgery. And then the diagnosis need to be confirmed by surgical pathology. Recently, a 42 year-old woman visited due to severe constipation. A flexible sigmoidoscopy revealed submucosal tumor on rectosigmoidal juction 20 cm above the anal verge. The surgical resection was performed and the biopsy showed the endomtriosis involving mucosa, submucosa, muscularis, serosa, subserosa and lymph node.


Asunto(s)
Adulto , Femenino , Humanos , Biopsia , Ciego , Colon , Estreñimiento , Diagnóstico , Endometriosis , Íleon , Incidencia , Corea (Geográfico) , Ganglios Linfáticos , Membrana Mucosa , Patología Quirúrgica , Membrana Serosa , Sigmoidoscopía
4.
Journal of Korean Society of Endocrinology ; : 76-81, 2004.
Artículo en Coreano | WPRIM | ID: wpr-115020

RESUMEN

Fifteen percent of patients with Cushing's syndrome could be accompanied with nonpituitary tumors that secrets ACTH-the ectopic ACTH syndrome. Among them, bronchial carcinoid is one of the rare causes of the ectopic ACTH syndrome. We experienced a 60-year-old woman who showed conditions of weight gain, generalized edema, hypokalemia, diabetes mellitus, and right middle lung mass. Histologically, the tumor was diagnosed with bronchial carcinoid and was confirmed as an ectopic ACTH syndrome through immunohistochemical staining of ACTH. After resection of the lung mass, blood sugar, electrolytes, generalized weakness, and blood pressure improved.


Asunto(s)
Femenino , Humanos , Persona de Mediana Edad , Síndrome de ACTH Ectópico , Hormona Adrenocorticotrópica , Glucemia , Presión Sanguínea , Tumor Carcinoide , Síndrome de Cushing , Diabetes Mellitus , Edema , Electrólitos , Hipopotasemia , Pulmón , Aumento de Peso
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA