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박용훈,하정옥,신정애,신손문,남해주 대한신장학회 1990 Kidney Research and Clinical Practice Vol.9 No.2
Glomerulocystic kidney, a rare form of nonfamilial cystic disease characterized by dilatation of Bownans space and adjacent tubules, is pathologically distinct from other renal cystic disease. This is very rare and combined with classic pathologic features and progressive impairment of renal function in some patients. We experienced a case of glomerulocystic disease in a male newborn baby with huge abdominal mass at left side who died within 15 hours after birth during treatment of hyaline membrane disease and persistent fetal circulation. Glomerulocystic kidney disease might be considered one of cystic renal disease in patient with abdominal mass.
노진우(Jin Woo Roh),이상춘(Sang Choon Lee),이수정(Soo Jung Lee),권굉보(Koing Bo Kwun),남해주(Hae Joo Nam) 대한두경부종양학회 1990 대한두경부 종양학회지 Vol.6 No.2
Squamous cell carcinoma of the thyroid gland is an extremely rare primary neoplasm, comprising only 1.1% of all primary thyroid cancers. The cancer is characterized by rapidly progressive clinical course in spite of its differentiated morphologic feature. Histogenetic origin of the cancer has also been debated. In most cases, a squamous epithelium is believed to be a result of metaplasia of a follicullar epithelium, although in rare exceptions, it can originate from a remnant of the thyroglossal duct or ultimobrachial body. Squamous cell carcinoma of the thyroid can occur in a pure form or mixed with adenocarcinoma; the latter may be designated as adenoacanthoma. Because this lesion typically runs a fulminant course, radical surgical resection at the earliest opportunity offers the best hope for cure. The lesions are usually radioresistant, and chemotherapy has not been shown to alter the course of this disease. We experienced a case of squamous carcinoma of the thyroid. This report summarize our experience and review of the literatures.