1.A Case of Nodular Amyloidosis.
Ho Su CHUN ; Duk Kyu CHUN ; Kwang Hyun CHO ; Hee Chul EUN ; Yoo Shin LEE
Annals of Dermatology 1992;4(2):113-116
A 65-year-old female patient visited our clinic complaining of multiple skin lesions since one year ago. There were yellowish to brownish colored, bean to walnut-sized nodules on both lower extremities. Dylon stain with polarizing microscopy, immunohistochemical stain to amyloid P and immunoglobuhn-kappa chain showed positive reactivities but keratin stain was negative. According to histopathologic and immunohistochemical findings, she was diagnosed as nodular amyloidosis.
Aged
;
Amyloid
;
Amyloidosis*
;
Female
;
Humans
;
Lower Extremity
;
Microscopy
;
Skin
2.A Case of Steroid-induced Atrophy of External Genitalia.
Jee Hyun JEON ; Jee Min PARK ; Eun Gyong YOO ; Duk Hee KIM
Journal of Korean Society of Pediatric Endocrinology 2001;6(2):160-164
Skin atrophy is one of the most common side effects of topical steroid use and results from decreased skin proalphaI collagen mRNA production due to specific alterations in collagen gene transcription or from reduced collagen mRNA stability. This report describes a case of a 8 year-old-girl who visited our hospital with a complaint of ambiguous genitalia. She was observed to have atrophic labia majora and atrophic striae resembling scrotal rugae. However, her serum levels of FSH, LH, 17-KS, 17-OHCS, 5-DHT, DHT and DHEA-S were all in normal range and her karyotype was 46,XX. Abdominal and pelvic ultrasonogram showed a normal uterus and ovaries. Careful history taking revealed frequent use of steroid ointment due to vulvar pruritus for 2 years and she was finally diagnosed to have atrophy of external genitalia induced by long-term use of topical steroid.
Atrophy*
;
Collagen
;
Disorders of Sex Development
;
Female
;
Genitalia*
;
Karyotype
;
Ovary
;
Pruritus
;
Reference Values
;
RNA Stability
;
RNA, Messenger
;
Skin
;
Ultrasonography
;
Uterus
3.A Case of Multiple Skeletal Tuberculosis with Spina Ventosa: A Case Report
Byung Duk PARK ; Dong Hae KIM ; Hyun Gyu KIM ; Kyung Soo YOO
The Journal of the Korean Orthopaedic Association 1976;11(2):220-224
A case of multiple skeletal tuberculosis with spina ventosa proved by radiological and pathologicaI methods in 3 year old Korean male child is reported. It was treated with antituberculous chemotherapy (triple method of PAS, INAH, streptomycin). At follow up check within 2 years, we obtained good healing process without other complication.
Child
;
Drug Therapy
;
Follow-Up Studies
;
Humans
;
Male
;
Methods
;
Tuberculosis
4.Clinicopathologic analysis on 25 cases of giant cell tumor of bone.
Hyun Ki YOUN ; Seung Seok SEO ; Hyun Duk YOO ; Young Chang KIM ; Jang Seok CHOI ; Young Goo LE
The Journal of the Korean Orthopaedic Association 1993;28(6):2256-2264
No abstract available.
Giant Cell Tumor of Bone*
;
Giant Cell Tumors*
;
Giant Cells*
5.Roles of Nitric Oxide and Tumor Necrosis Factor in Liver Inloammation Induced by C . parvum and LPS.
Ji Chang YOO ; Hyun Ock PAE ; Hun Taeg CHUNG ; Chang Duk JUN ; Yoo Hyun KIM ; Shin Moo KIM ; Rae Kil PARK ; Hyo Sang JIN
Korean Journal of Immunology 1998;20(2):237-243
No abstract available.
6.The Influence of Rotatory Movement on the Tissue Catecholamines in Rats.
Duk Hyun LEE ; Chong Sup YOO ; Sa Suk HONG ; Woo Choo LEE
Yonsei Medical Journal 1968;9(2):93-99
The present study was designed to examine the possible relationship between the function of the labyrinth and the role of the sympathetic nervous system In experimental motion sickness produced by rotatory movement(8O r.p.m.). The catecholamines in the brain, the heart and the adrenal gland of rats were rapidly reduced to one half of normal values following exposure to rotatory movement. The pretreatment with streptomycin and dramamine completely prevented the depletion by the rotatory movement of the catecholamines in the brain, the heart and the adrenal gland, but scopolamine did not prevent the decrease. Bretylium or chlorpromazine signifcantly inhibited reduction of the catechol-amines in both of the brain and the heart. However they did not influence the decrease in the adrenal gland. The reduction of the tissue catecholamines in rotatory movement is presumed to be caused largely by activation of the sympathetic nervous system mediated through labyrinthine stimulation.
Animals
;
Catecholamines/*metabolism
;
Labyrinth/*physiopathology
;
Male
;
Motion Sickness/*etiology
;
Rats
;
*Rotation
;
Sympathetic Nervous System/*physiopathology
;
OID - NASA: 70030571
7.A Case of Guillain-Barr Syndrome Complicated by Persistent Hypertension.
Jung Hyun KIM ; Kyung Tae HWANG ; Kyong Og KO ; Yun Duk YOO
Journal of the Korean Child Neurology Society 1999;7(1):124-128
Guillain-Barr syndrome is rarely complicated by hypertension, which has been ascribed to sympathetic nervous system hyperactivity. We report a 11 years old female with Guillain-Barr syndrome complicated by persistent hypertension associated with elevated renin-angiotensin. So we report this case with brief review of related literatures.
Child
;
Female
;
Humans
;
Hypertension*
;
Sympathetic Nervous System
8.A Case of Generalized Meconium Peritonitis without Peritoneal Calcification.
Kyung Tae HWANG ; Jung Hyun KIM ; Kyong Og KO ; Yun Duk YOO
Journal of the Korean Society of Neonatology 1998;5(2):232-236
Neonatal ascites is an uncommon problem with many etiologies. The common causes include hematologic diseases, bowel perforation, obstructive uropathy, cardiovascular diseases, chylous ascites, intrauterine infection, and meconium peritonitis. Recently, the wide application of sonography has greatly narrowed the list of differential diagnosis of neonatal ascites. Meconium peritonitis is readily diagnosed if calcification in the abdomen or scrotum can be seen radiologically or sonographically in a neonate with abdominal distension at birth. We report a case of generalized meconium peritonitis without intraabdominal calcification by radiologic and sonographic study and notable meconium hydrocele at birth.
Abdomen
;
Ascites
;
Cardiovascular Diseases
;
Chylous Ascites
;
Diagnosis, Differential
;
Hematologic Diseases
;
Humans
;
Infant, Newborn
;
Meconium*
;
Parturition
;
Peritonitis*
;
Scrotum
;
Ultrasonography
9.Clinical Course and Treatment of Early Neonatal Hypocalcemia.
Kyung Tae HWANG ; Jung Hyun KIM ; Kyong Og KO ; Yun Duk YOO
Journal of the Korean Society of Neonatology 1998;5(2):172-181
PURPOSE: The clinical findings of early neonatal hypocalcemia are variable and it is difficult to find relationship between the symptoms and hypocalcemia due to complex causes. The purpose of this study is to establish the relationship between early neonatal hypocalcemia and clinical manifestations and to propose a guideline for appropriate treatment of early neonatal hypocalcemia, especially in asymptomatic cases. METHODS: Study subjects were all sick babies admitted to nursery and NICU and randornly selected 43 healthy babies at Sun General Hospital from January 1996 to December 1996. We examined serum calcium level within 72 hours after birth. Then we evaluated prospectively clinical findings according to each disease category in hypocalcemic cases and analysed the relationship of time course of clinical findings with hypocalcemia and compared serum calcium concentration followed by each therapy after 3 days. RESULTS: The results were as follows. 1) The incidence of early neonatal hypocalcernia was high in premature infants, low birth weight infants, infants with neonatal asphyxia, hyaline membrane disease and transient tachypnea. 2) Tremor, seizure, apnea, dyspnea, abdominal distension, cyanosis, and vomiting were frequently presented symptoms in early neonatal hypocalcemia. 3) In the cases of early hypocalcemia with symptoms, these symptoms persisted continuously after norrnalization of serum calcium concentration. 4) Among asymptomatic hypocalcernic group, mean serum calcium levels changed from 6.7 mg/dL to 8.7 mg/dL in 23 cases of no treatment, from 5.4 mg/dL to 10.3 mg/dL in 4 cases of calcium gluconate infusion, and from 6.3 mg/dL to 8.7 mg/dL in 7 cases of feeding low phosphorus containing milk. None persisted in hypocalcemic state irrespective of treatment methods. CONCLUSION: It is difficult to regard these symptoms as a rule to treatment because these symptoms were present after normalizaton of serum calcium concentration. In addition, asymptomatic hypocalcemia was improved shortly without any treatment without any problem. We conclude that for asymptomatic hypocalcemia, withholding dangerous calcium gluconate infusion would be perrnissible.
Apnea
;
Asphyxia
;
Calcium
;
Calcium Gluconate
;
Cyanosis
;
Dyspnea
;
Hospitals, General
;
Humans
;
Hyaline Membrane Disease
;
Hypocalcemia*
;
Incidence
;
Infant
;
Infant, Low Birth Weight
;
Infant, Newborn
;
Infant, Premature
;
Milk
;
Nurseries
;
Parturition
;
Phosphorus
;
Prospective Studies
;
Seizures
;
Solar System
;
Tachypnea
;
Tremor
;
Vomiting
10.Subacute Progressive Ascending Myelopathy: A case report.
Journal of the Korean Academy of Rehabilitation Medicine 2010;34(5):595-598
Subacute progressive ascending myelopathy is a rare condition complicating spinal cord injury, unrelated to mechanical compression, instability, hemorrhage or syrinx formation. Clinically, ascending neurological deficit may extend at least two segments above the level established at the initial insult within the first 3 weeks of the initial spinal cord insult. MR imaging characteristically demonstrates cord changes ascending at least four vertebral levels above the initial injury site. The development of progressive myelopathy is a dreaded complication of spinal cord injury and is not misunderstood for post-op complication. We describe a case of a 29-year-old male patient who suffered a falling down accident. He initially presented with a T12 vertebral fracture with associated cord compression and signal changes in the spinal cord. During the subsequent 3 weeks, he developed progressive sensory changes with cord signal abnormalities on magnetic resonance imaging extending above from the injury site.
Adult
;
Hemorrhage
;
Humans
;
Magnetic Resonance Imaging
;
Male
;
Spinal Cord
;
Spinal Cord Diseases
;
Spinal Cord Injuries