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1.
Korean Journal of Urology ; : 1110-1112, 2005.
Artículo en Coreano | WPRIM | ID: wpr-111364

RESUMEN

A lymphoma of the prostate is very rare, and is usually incidentally discovered. Malignant lymphomas can be divided into either primary or secondary according to their origin. Secondary involvement of the gland is the most common presentation. Most non-Hodgkin's lymphomas that affect the prostate are of the B-cell type, and present with non-specific obstructive symptoms. A variety of methods have been used for their, including prostatectomy, radiotherapy or combinations of chemotherapy and radiotherapy. However, the prognosis remains poor, regardless of the patient's age, histological type, treatment or clinical stage at presentation. Here, the case of a patient with a B-cell lymphoma, who presented with symptoms of a bladder outlet obstruction, is reported. The patient has been in complete remission following the completion of 6 cycles of doxorubicin-based chemotherapy and accompanying radiotherapy.


Asunto(s)
Humanos , Linfocitos B , Quimioterapia , Quimioterapia Combinada , Linfoma , Linfoma de Células B , Linfoma no Hodgkin , Pronóstico , Próstata , Prostatectomía , Radioterapia , Obstrucción del Cuello de la Vejiga Urinaria
2.
Korean Journal of Urology ; : 1113-1115, 2005.
Artículo en Coreano | WPRIM | ID: wpr-111363

RESUMEN

Penile metastases are rare, and usually secondary to other genitourinary primary tumors. Bladder, prostate and renal tumors are the main sources of penile metastasis. Rectal and respiratory neoplasms also metastasize to the penis. However, metastatic penile cancer originating from the pancreas is extremely rare. Here, a case of pancreatic cancer, with penile metastasis, is reported.


Asunto(s)
Masculino , Metástasis de la Neoplasia , Páncreas , Neoplasias Pancreáticas , Neoplasias del Pene , Pene , Próstata , Vejiga Urinaria
3.
Korean Journal of Pediatric Gastroenterology and Nutrition ; : 47-55, 2000.
Artículo en Coreano | WPRIM | ID: wpr-112812

RESUMEN

PURPOSE: The aim of this research is to examine the abnormal liver function complicated with Kawasaki disease (KD) and to analyze its clinical characteristics and complications. METHODS: Ninty eight cases were diagnosed as having KD, among which thirty four cases had abnormal alanine aminotransferase (ALT) (>30 IU/L). These abnormal ALT cases were evaluated in terms of age and sex distribution, major symptoms, complications, laboratory and histopathologic findings. RESULTS: Male to female ratio was 2.4 : 1 and most patients (91.2%) were under 5 years of age. Cervical lymphadenopathy was observed in 3 cases (8.8%); and recurred cases were two (5.8%). Average fever duration was 8 days: average length of hospitalization was 9 days; and average recovery period was 13 days. Immediately after admission, positive CRP was observed in 31 cases (91.2%), leukocytosis (>10,000/mm(3)) in 26 cases (76.0%), thrombocytosis (>450,000/mm(3)) in 7 cases (20.6%), and anemia (<10 gm/dl) in 7 cases (20.6%), respectively. GB hydrops or cholecystitis were noted in 3 cases (8.8%) abnormal ECG finding in 1 case (2.9%), coronary dilatation or aneurysm in 2 cases (5.9%). Liver biopsy was done in four cases and revealed mild infiltration of lymphocytes on the portal area and mild bile duct proliferations. CONCLUSION: The abnormal liver function was noted in 34.7% of KD patients, and subsided all within one month. But the liver function test should be checked closely in patients of the abnormal liver function test complicated with KD despite of its good prognosis.


Asunto(s)
Femenino , Humanos , Masculino , Alanina Transaminasa , Anemia , Aneurisma , Conductos Biliares , Biopsia , Colecistitis , Dilatación , Edema , Electrocardiografía , Fiebre , Hospitalización , Leucocitosis , Pruebas de Función Hepática , Hígado , Enfermedades Linfáticas , Linfocitos , Síndrome Mucocutáneo Linfonodular , Pronóstico , Distribución por Sexo , Trombocitosis
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