2.Pneumatosis intestinalis after adult liver transplantation.
Jong Man KIM ; Yulri PARK ; Jae Won JOH ; Choon Hyuck David KWON ; Sung Joo KIM ; Seung Heui HONG ; Suk Koo LEE
Journal of the Korean Surgical Society 2011;80(Suppl 1):S47-S50
Pneumatosis intestinalis is an uncommon disorder characterized by an accumulation of gas in the bowel wall. We described three cases undertaking liver transplantation. The patients developed diarrhea in three cases and high fever in two. An abdominal X-ray and computed tomography scan demonstrated extensive pneumatosis intestinalis in the colon with pneumoperitoneum mimicking hollow organ perforation. However, the patients had no abdominal symptoms and there was no evidence of peritonitis. The infection work-up was negative except one case with cytomegalovirus antigenemia. After one week of conservative management including bowel rest and antibiotic therapy, their pneumoperitoneum resolved spontaneously without any complication. Pneumatosis intestinalis should be considered as a differential diagnosis after adult liver transplantation with patients suffering from watery diarrhea and fever. Pneumoperitoneum, air-density in mesentery and retroperitoneum in patients with pneumatosis intestinalis without signs of peritonitis improved with conservative management, which included bowel rest and antibiotic therapy.
Adult
;
Colon
;
Cytomegalovirus
;
Diagnosis, Differential
;
Diarrhea
;
Fever
;
Humans
;
Liver
;
Liver Transplantation
;
Mesentery
;
Mortuary Practice
;
Peritonitis
;
Pneumoperitoneum
;
Stress, Psychological
3.Neonatal vitelline vein aneurysm with thrombosis: prompt treatment should be needed.
Soo Hong KIM ; Hyeong Won YU ; Hyun Young KIM ; Heui Seung JO
Annals of Surgical Treatment and Research 2015;89(6):334-337
Vitelline veins are a pair of embryonic structures. The veins develop the portal vein system. Serious problems occur if the vitelline vein does not regress and becomes an aneurysm. Thrombus formation in the vitelline vein aneurysm could lead to portal vein thrombosis and portal hypertension unless promptly and correctly treated. Though vitelline vein aneurysm is an extremely rare anomaly, it rapidly progresses to portal vein thrombosis that requires prompt diagnosis and treatment. We reported a case of neonatal vitelline vein aneurysm and thrombosis that was cured by prompt operation.
Aneurysm*
;
Diagnosis
;
Embryonic Structures
;
Humans
;
Hypertension, Portal
;
Infant, Newborn
;
Portal Vein
;
Thrombosis*
;
Veins*
;
Venous Thrombosis
;
Vitellins*
4.Adult intussusception caused by inverted Meckel's diverticulum treated with operation.
Sung Yun LEE ; Jae Yoon JEONG ; Seung Hyun HONG ; Seung Min WOO ; Su Heui LEE ; Hyun Joo YOU ; Dong Won KIM
Yeungnam University Journal of Medicine 2016;33(2):116-119
Intussusception is a serious disease where part of the intestine slides into an adjacent part of the intestine. Adult intussusception is mainly due to benign or malignant neoplasm. Therefore, in most cases of adult intussusception, treatment by surgery would be preferable to conservative therapy. However, we report on a 28-year-old female patient who underwent intussusception operation delayed 3 months. Abdominal computed tomography 3 months ago showed a small bowel intussusception measuring 20 cm long. Three months later, the previously identified small bowel intussusception appeared without change. The patient underwent surgery, and ectopic gastric mucosa was observed in the biopsy. Therefore, Meckel's diverticulum was diagnosed.
Abdominal Pain
;
Adult*
;
Biopsy
;
Female
;
Gastric Mucosa
;
Humans
;
Intestines
;
Intussusception*
;
Meckel Diverticulum*
5.A Case of Fulminant Type 1 Diabetes Mellitus in an Elderly Patient.
Seung Min WOO ; Seung Hyun HONG ; Sung Yun LEE ; Su Heui LEE ; Duc Ky LEE ; Sae Jeong YANG
Journal of Korean Diabetes 2015;16(3):225-229
Insulin deficiency due to destruction of pancreatic beta-cells is a typical characteristic of type 1 diabetes mellitus (DM). In 2000 Imagawa proposed a novel diagnostic model defining "fulminant type 1 DM" as developing rapidly without any evidence of autoimmunity, and ever since there have been many reports regarding the matter in Japan. In 2004, the first fulminant type 1 diabetes case was reported in Korea; however, there have been few reports since then. We present a case of a 60-year-old man who suffered from excessive thirst and polyuria after myalgia. Laboratory findings revealed a high blood glucose level and evidence of diabetic ketoacidosis, but the HbA1c level was within the normal range. The serum C-peptide level was very low and antibodies to glutamic acid decarboxylase were negative. These findings suggested fulminant type 1 diabetes. This patient has shown improvement in symptoms and examination results without complications after being treated with insulin therapy with hydration, throughout 6-months follow-up period.
Aged*
;
Antibodies
;
Autoimmunity
;
Blood Glucose
;
C-Peptide
;
Diabetes Mellitus
;
Diabetes Mellitus, Type 1*
;
Diabetic Ketoacidosis
;
Follow-Up Studies
;
Glutamate Decarboxylase
;
Humans
;
Insulin
;
Japan
;
Korea
;
Middle Aged
;
Myalgia
;
Polyuria
;
Reference Values
;
Thirst
7.Type Distribution of Unexpected Red Cell Antibodies in Patients with Malignancy.
Chang Eun YOON ; Jin Kyung LEE ; Young Jun HONG ; Seok Il HONG ; Bo You YUN ; Heui Seung JO ; Yoon Hwan CHANG
Korean Journal of Blood Transfusion 2012;23(1):58-67
BACKGROUND: Performance of antibody screening and identification tests before blood transfusion is important because the unexpected presence of red cell antibodies may cause hemolytic transfusion reactions. Many patients with malignancy undergo transfusion in order to overcome pancytopenia due to disease itself or chemotherapy. We investigated the type distribution of unexpected red cell antibodies in cancer patients and compared our results with those of other institutions. METHODS: From January 2008 to June 2011, 30,989 serum samples were screened using a LISS/Coombs card and ID-DiaCell I, II (DiaMed AG, Morat, Switzerland). Data-Cyte Plus Reagent Red Blood Cells (Medion Diagnostics, Dudingen, Switzerland) were used in performance of antibody identification tests. RESULTS: Out of 30,989 serum samples, 180 cases (0.58%) showed screening-positive results, and unexpected antibodies were identified in 72 cases. The type of unexpected antibody observed most often in cancer patients was a member of the Rh antibody group, anti-E in 17 cases (29.8%), followed by anti-Lea in five cases (8.8%) and anti-e in three cases (5.3%). While Rh group antibodies were observed in the colon cancer group, non-Rh group antibodies were observed in the rectal cancer group. And, in the genitourinary cancer group, Lewis group antibodies were more frequently detected than others. CONCLUSION: Findings from our study demonstrated a type distribution of unexpected red cell antibodies that was similar to those reported in previous studies. Compared with non-cancerous patients, no difference in type distribution of unexpected red cell antibodies was observed in cancer patients. Some antibodies were frequently observed in certain cancer groups. Further comprehensive research on unexpected antibodies based on location or histologic type of cancer is needed.
Antibodies
;
Blood Group Incompatibility
;
Blood Transfusion
;
Colonic Neoplasms
;
Erythrocytes
;
Humans
;
Mass Screening
;
Pancytopenia
;
Rectal Neoplasms
;
Urogenital Neoplasms
8.Treatment of Severe Small Bowel Involvement in Henoch-Schonlein Purpura: Two Cases Report.
Hyung Tae KIM ; Jin Soo MOON ; Hyun Oh JANG ; Heui Seung JO ; Jong Guk LEE ; Ki Hong KIM ; Jung Wook SEO ; Min Kyung KIM
Korean Journal of Pediatric Gastroenterology and Nutrition 2004;7(1):78-82
Henoch-Schonlein purpura (HSP) is a vasculitis of the small vessels in skin, joints, gastrointestinal (GI) tract and kidney. GI symptoms occur in up to 85% of patients and may lead to severe problems such as intussusception, obstruction, and perforation. GI symptoms may not be easily controlled, showing refractoriness to the conventional corticosteroid therapy. Although GI involvements of HSP are acute, and self-limited in most instances, they may cause fatal results in some unusual cases. In such conditions all the possible therapeutic modalities should be considered. We report two cases of severe small bowel involvement of HSP. One case presented with severe abdominal pain showing refractoriness to corticosteroid, but improved with IV immunoglobulin therapy. In the second case, HSP with transmural infarction in the small bowel could be cured with surgical intervention.
Abdominal Pain
;
Humans
;
Immunization, Passive
;
Immunoglobulins
;
Infarction
;
Intussusception
;
Joints
;
Kidney
;
Purpura, Schoenlein-Henoch*
;
Skin
;
Vasculitis
9.The Sagittal Balance of Cervical Spine : Comprehensive Review of Recent Update
Sang Hoon LEE ; Tae Hwan KIM ; Seok Woo KIM ; Hyun Take RIM ; Heui Seung LEE ; Ji Hee KIM ; In Bok CHANG ; Joon Ho SONG ; Yong Kil HONG ; Jae Keun OH
Journal of Korean Neurosurgical Society 2023;66(6):611-617
The cervical spine plays a critical role in supporting the skull, maintaining horizontal gaze, and facilitating walking. Its unique characteristics, including the widest range of motion among spinal segments, have led to extensive research on cervical sagittal alignment. Various parameters have been proposed to evaluate cervical alignment, with studies investigating their clinical significance, correlation with symptoms, and implications for surgical interventions. Recent findings suggest that cervical sagittal alignment not only impacts the cervical spine but also influences global spine-pelvic alignment through compensatory mechanisms. This comprehensive review examines classical and new parameters of cervical sagittal alignment and considers the dynamic and muscular factors associated with it.
10.A Case of Citrullinemia Diagnosed at the Neonatal Period.
Seung Kyu SONG ; Kyung Chang OH ; Mi Ae HONG ; Hee Taeg KIM ; Hye Jung SHIN ; Soon Young KIM ; Jin Keun CHANG ; Heui Seung JO ; Beyong Il KIM ; Sei Won YANG ; Jung Hwan CHOI
Journal of the Korean Pediatric Society 2002;45(4):524-528
Citrullinemia is a rare inborn error of metabolism of the urea cycle, and was first reported by McMurray, et al. in 1962. It is inherited as an autosomal recessive trait. The normal synthesis of argininosuccinic acid is blocked in this disease due to a deficiency of argininosuccinic acid synthetase(AS), which has been demonstrated in liver cells and fibroblasts. The clinical symptoms are vomiting, lethargy or irritability, convulsion and mental retardation. The diagnosis is made by the finding of an increased plasma citrulline level. Every effort should be made to reduce the blood ammonia level as rapidly as possible before irreversible brain damage occurs. This report describes a case of citrullinemia that was diagnosed through organic acid analysis and amino acid analysis, and reviews the related literatures.
Ammonia
;
Argininosuccinic Acid
;
Brain
;
Citrulline
;
Citrullinemia*
;
Diagnosis
;
Fibroblasts
;
Intellectual Disability
;
Lethargy
;
Liver
;
Metabolism
;
Plasma
;
Seizures
;
Urea
;
Vomiting