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증례 : 상부 위장관의 부분적 선천성 전위의 1 예보고
조준탁 ( Joon Tack Cho ),김치억 ( Chi Uk Kim ),신용후 ( Yong Hoo Shin ),하창우 ( Chang Woo Ha ),양경호 ( Kyuang Ho Yang ) 대한내과학회 1968 대한내과학회지 Vol.11 No.10
A case of congenital partial situs inversus of upper gastrointestinal tract (stomach and duodenum) without dextrocardia was presented. The literatures on the partial situs inversus were reviewed.
조준탁 ( Joon Tack Cho ),박광용 ( Kwang Yong Park ),김영선 ( Young Sun Kim ),이안기 ( Ahn Ki Lee ),주장복 ( Chang Bok Joo ),김우열 ( Woo Youl Kim ),김광회 ( Kwang Hoi Kim ) 대한내과학회 1970 대한내과학회지 Vol.13 No.2
Clinical study was done on 21 cases of pericarditis admitted to Capital Army Hospital from January 1964 to June 1968, and following results were obtained. 1) Tuberculosis was the most frequent cause (over 40%), and acute nonspecific, neoplastic, bacterial
조준탁 ( Joon Tack Cho ),박광용 ( Kwang Yong Park ),김영선 ( Young Sun Kim ),주장복 ( Chang Bok Joo ),김우열 ( Woo Youl Kim ),김광회 ( Kwang Hoi Kim ),정주일 ( Joo Il Chung ),박진영 ( Jin Young Park ) 대한내과학회 1970 대한내과학회지 Vol.13 No.2
Two cases of postural heart block were presented and the possible mechanisms were discussed in accordance with literature. Case I was 23 years old soldier admitted to cardiologic department of Capital Army Hospital via emergency room because of Adams-Stoke
부분적인 Albright 의 선천성 골이영양증을 동반한 위부갑상선기능 저하증 1 예
고병구(Byoung Goo Ko),홍석구(Seok Gu Hong),진성호(Sung Ho Jin),박동철(Dong Chul Park),조준탁(Joon Tack Cho),이진관(Jin Kwan Lee) 대한내과학회 1986 대한내과학회지 Vol.31 No.1
N/A Pseudohypoparathyroidism is a genetic disorder characterized by target cell resistance to the effects of parathyroid hormone, In general the patients have hypocalcemia, hyperphosphosphathemia, elevated serum PTH level and a characteristic appearance termed Albright's hereditory osteodystrophy(AHO), The disorder is classified to type I and type g. Type I PsHP is subclassified to type la and type lb. Type Ia PsHP shows deficient G unit activity in target cell membrane and associated with other endocrine abnormalities and AHO in common. Type Ib PsHP shows normal G unit activity but deficient urinary cyclic AMP responce. Type Ⅱ PsHP shows normal c-AMP response to PTH, but also shows target cell resistance to PTH. We experienced a case of pseudohypoparathyroidism in 18 year old girl who had had frequent carpopedal spasm and generalized seizure for about 4 years. She had very low serum calcium level(3.8 mg/dL) and high immunoreactive PTH level(720 pg/ml), Even though every feature of AHO was not fulfilled, she had round face, short neck and obese stature. But she didn't have brachydactyly and subcutaneous calcification. She had no other endacrine abnormality but showed borderline mental retardation in IQ test. This case was of particular interest in that she showed incomplete presentation of AHO with pseudohypoparathyroidism.
진성호,박동철,이진관,고병구,홍석구,조준탁 대한내과학회 1986 대한내과학회지 Vol.31 No.6
Bacterial thyroiditis is a very uncommon disease caused most often by gram positive cocci such as Staphylococcus aureus, Streptococus pyogenes and Streptococcus pneumoniae. Primary actinomycosis of the thyroid is extremely rare. Since the first report in 1894, twelve patients have been described in Western literature. Bacause of infrequent occurrence and atypical presentation the clinical diagnosis of actinomycosis is very difficult, particulary in the thyroid gland. We experienced a case of actinomycosis of the thyroid in 48 year old farmer who had slowly growing hard mass in right anterior aspect of neck. On provisional diagnosis of thyroid carcinoma subtotal thyroidectomy and right anterior neck dissection was done. Histopathology showed acute and chronic inflammation with necrosis, abscess formation and 'sulfur granules' in right lobe of thyroid which were thought to be characteristic features of actinomycosis of the thyroid.
진성호,박동철,이진관,고병구,홍석구,조준탁 대한내과학회 1986 대한내과학회지 Vol.31 No.6
Central diabetes insipidus is a polyuric disorder that results from a lack of sufficient ADH to effect appropriate concentration of the urine for water conservation. It is divided into primary and secondary diabetes insipidus. The majority of secondary diabetes insipidus is caused by operation, neoplastic lesions of the pituitary and hypothalamus and head trauma. Secondary diabetes insipidus complicated with tuberculous meningitis is extremely rare. There have been several reports on diabetes insipidus but no reports on the disorder associated with tuberculous meningitis in Korea. We reported a patient of 38 year old male who developed diabetes insipidus during treatment of tuberculous meningitis and active pulmonary tuberculosis. Tuberculous meningitis was documented by clinical features, laboratory findings and therapeutic response, even though AFB smear of the cerebrospinal fluid was negative in the patient. Water deprivation and pitressin injection test revealed complete type of diabetes insipidus. We have followed this patient's status of diabetes insipidus up for one half year and he has been on 5 units of pitressin tannate in oil every 3 to 4 days. We think his status of diabetes insipidus in permanent.