1.A Case of Double Pylorus Associated with Chronic Bronchitis and Gastric Ulcer.
Young Chan LIM ; Beoung Ho HAN ; Dong Whee CHO ; Jae Rack HONG ; Tae Hee JUN ; Hong Seub LIM ; Young Woong SHIM ; Gap Young SONG
Korean Journal of Gastrointestinal Endoscopy 2002;25(2):89-91
The double pylorus is a fistulous communication between gastric antrum and duodenal bulb. It appears to be an acquired lesion in the majority of cases. Upon routine endoscopic procedures, it is frequently seem to occur in males who are either alcoholics, diabetics, those with chronic renal failure, chronic lung disease. If it is no developing complications such as septal rupture, double pylorus is well response to medical treatment. A 51-year-old man who had been taking medication over a long period for the chronic bronchitis was admitted to this hospital because of epigastric soreness and indigestion for 1 month. Endosopic findings showed two large openings of the pyloric channel and gastric ulcer in the channel. We thought that this case was an acquired lesion reasult of repeated gastric ulcer. We report a case of double pylrous with the brief review of literatures.
Alcoholics
;
Bronchitis, Chronic*
;
Dyspepsia
;
Humans
;
Kidney Failure, Chronic
;
Lung Diseases
;
Male
;
Middle Aged
;
Pyloric Antrum
;
Pylorus*
;
Rupture
;
Stomach Ulcer*
2.A Case of Primary Amenorrhea due to 17 -Hydroxylase Deficiency.
Hong Seub RIM ; Seon Hwa LEE ; Jung Min HONG ; Jae Hyun NAM ; Hee Back PARK ; Chul Woo AN ; Do Min KI ; Sung Kil LIM ; Young Duk SONG ; Hyun Chul LEE ; Kap Bum HUH ; Inn Soo KANG
Journal of Korean Society of Endocrinology 2001;16(1):130-133
17 -Hydroxylase deficiency is a rare form of congenital adrenal hyperplasia that is characterized by primary amenorrhea, absence of secondary sex characteristics, hypertension, and a hypokalemic alkalosis that has resulted resulting from increased production of deoxycorticosterone and corticosterone by the adrenal. The diagnosis of this enzyme deficiency can be recognized by the increasing serum concentrations of steroid precursors, DOC and corticosterone and the decreasing concentrations of cortisol, and adrenal androgens. We diagnosed this in a 19 year old female who presented with primary amenorrhea. We report this case with a review of the literatures.
Adrenal Hyperplasia, Congenital
;
Alkalosis
;
Amenorrhea*
;
Androgens
;
Corticosterone
;
Desoxycorticosterone
;
Diagnosis
;
Female
;
Humans
;
Hydrocortisone
;
Hypertension
;
Sex Characteristics
;
Young Adult