1.Huge Peripelvic Lymphatic Cyst: A Case Report.
Kang Woo EUH ; Young Woo KONG ; Hi Chu SONG ; Kee Soo KIM
Korean Journal of Urology 1978;19(5):461-464
Peripelvic lymphatic cyst or the kidney is a rare case in Korean Urological literature. We have experienced a case of it in 30 years old woman who had a palpable fluctuant mass in the upper right quadrant of the abdomen. The operated cyst was dark-red colored appearance and filled with amber colored fluid about 800cc. We have removed it together with kidney. The cyst measured 200gm. in weight, 10 x 5 x 4.5 cm in size and 0.5cm thickness of the cystic wall. Histological finding of the cystic wall showed a consisting of endometrial cell underlying tissue was collagen fiber and fibrotic change. The fluid of cyst contained 98 % of lymphatic cell.
Abdomen
;
Adult
;
Amber
;
Collagen
;
Female
;
Humans
;
Kidney
;
Lymphocele*
2.Analysis of fluid in simple renal cyst.
Heung Jae PARK ; Duck Ki YOON ; Jae Heung CHO ; Sung Kun KOH
Korean Journal of Urology 1991;32(5):725-728
We assessed cyst fluid of 14 cases of simple renal cyst. The aspirates were analyzed for color, lipid. protein, glucose, lactic acid dehydrogenase(LDH), amylase, electrolytes and Papanicolaou smears and cell blocks were performed. A clear amber fluid with minimal lipid content, LDH lower than that of blood and a normal cell pattern on Papanicolaou stain and cell block which are characteristics of transudate were seen in all cases. Although the number of cases are insufficient, it would appear that the content of simple renal cyst is identical to that of transudate.
Amber
;
Amylases
;
Cyst Fluid
;
Electrolytes
;
Exudates and Transudates
;
Glucose
;
Lactic Acid
;
Papanicolaou Test
3.Dentinogenesis imperfecta type II: A case report with 17 years of follow-up.
Francisco José Reis GAMA ; Isabella Sousa CORRÊA ; Claudia Scigliano VALERIO ; Emanuelle de Fátima FERREIRA ; Flávio Ricardo MANZI
Imaging Science in Dentistry 2017;47(2):129-133
Dentinogenesis imperfecta is a dominant autosomal hereditary disorder of dentin formation that affects the deciduous and permanent teeth. Its etiology is characterized by inadequate cell differentiation during odontogenesis. The clinical characteristics of dentinogenesis imperfecta are discolored teeth with a translucency that varies from gray to brown or amber. Radiographically, the teeth exhibit pulp obliteration, thin and short roots, bell-shaped crowns, and periapical bone rarefaction. The aim of this report was to present a case of dentinogenesis imperfecta type II that was followed up over a 17-year period. This report also presents scanning electron microscopy images of the enamel and dentin, showing that both were altered in the affected teeth. The disease characteristics and the treatments that were administered are reported in this study to guide dentists with respect to the need for early diagnosis and adequate follow-up to avoid major sequelae.
Amber
;
Cell Differentiation
;
Crowns
;
Dental Enamel
;
Dentin
;
Dentinogenesis Imperfecta*
;
Dentinogenesis*
;
Dentists
;
Early Diagnosis
;
Follow-Up Studies*
;
Humans
;
Microscopy, Electron, Scanning
;
Odontogenesis
;
Tooth