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Case Report
Aplastic Crisis Secondary to Parvovirus B19 Infection
Yang Joon Park, Dae Kyun Koh, Jin Hee Oh
Clin Exp Pediatr. 2003;46(11):1139-1142.   Published online November 15, 2003
Human parvovirus(HPV) B19 infection causes erythema infectiosum in children, sometimes red cell aplastic crisis with hemolytic anemia and chronic bone marrow failure in immunocompromised hosts. HPV B19 is directly cytotoxic for erythroid progenitor cells and inhibits erythropoiesis. Infrequently, HPV B19 inhibits hematopoiesis of three cell lineages and causes transient pancytopenia in patients with hemolytic disorders. We report three patients with...
Original Article
Mean Corpuscular Hemoglobin Concentration as a Discriminating Tool between Hereditary Spherocytosis and Intravascular Hemolysis
Hae Young Park, Hwang Min Kim, Kyoung Ah Lee, Dong Il Won, Sei Myeng Park, Seok Won Park, Baek Keun Lim, Kil Young Kim
Clin Exp Pediatr. 2001;44(6):664-668.   Published online June 15, 2001
Purpose : The purposes of this study were to elucidate the diagnostic significance of mean corpuscular hemoglobin concentration(MCHC) for various kinds of hemolytic anemia, the mechanism of elevated MCHC in hereditary spherocytosis(HS). Methods : The subjects consisted of 39 cases of HS(group 1), 31 cases of intravascular hemolysis (IH) such as DIC, snake bite or hemolytic uremic syndrome(group 3), and sex...
One Case of Recovery Phase of Aplastic Crisis in Hereditary Spherocytosis with Family History.
Eun Kyung Won, Dong Hyeon Kim, Ho Seung, Chang Hee Choi
Clin Exp Pediatr. 1990;33(10):1434-1440.   Published online October 31, 1990
We experienced a case of hereditary spherocytosis patient who was in a recovery phase of aplastic crisis at the time of presentation. This was a 7 years old boy with complaints of pallor and intermit- tent abdominal pain. Asymptomatic jaundice was also found in the patient's grandfather and two maternal uncles. Patient’s mother had splenectomy due to hereditary spherocytosis. Diagnosis was made by morphology,...
A Clinical Study of Hereditary Spherocytosis.
Ki Ho Kim, Kun Soo Lee, Haeng Mi Kim, Doo Hong Ahn
Clin Exp Pediatr. 1990;33(1):81-87.   Published online January 31, 1990
The following results were obtained from eight cases of hereditary spherocytosis (HS) who were admitted at the Department of Pediatrics, Kyung-pook National University Hospital from July 1984 to January 1989. The percentage of HS among the pediatric hematology patients during the same period was 2.6%. Male amd female were one and seven respectively. The mean age at the diagnosis and at onset of symptom was...
Three Cases of hereditary Spherocytosis.
D H Kim, M Y Kim, S Y Kim, J Y Jung
Clin Exp Pediatr. 1988;31(4):500-505.   Published online April 30, 1988
We experienced 3 cases of herediatry spherocytosis which occurred in a family. The family consited of parents, one sone and one daughter. The case I, Daughter showed the chief complaints of pallor ad generalized weakness. The case II, Son hoswed the chief complaint of jaundice. The case III, Father showed the chief complaints of fatigue and dizziness. Diagnosis was made by presence of spherocytes in...
Clinical Observation on Splenectomized Children.
Mi Ryung Um, Jae Won Song, Yong Yull Koh, Jeong Kee Seo, Hyo Seop Ahn, Chang Yee Hong, Kwi Won Park
Clin Exp Pediatr. 1987;30(5):511-517.   Published online May 31, 1987
A clinical study was performed on 26 cases of splenectomized children who had been seen at the Department of Pediatrics, Seoul National University Hospital, during the period of 7 years 7 months from January 1978 to July 1985. The results were as follows: 1) Primary diseases were hereditary spherocytosis (8 cases), Hodgkin disease for staging laparotomy (8 cases), ...
Case Report
A Case of Hereditary Spherocytosis.
Yeon Kyun Oh, Byeong Ho Lee, Young Ha Kim, Moon Ki Cho
Clin Exp Pediatr. 1986;29(9):1021-1027.   Published online September 30, 1986
We experienced a case of hereditary spherocytosis in a 6 year 3 month old boy who complained of anemia and jaundice. The diagnosis was confirmed by spherocytes in peripheral blood, osmotic fragility test, autohemolysis test and bone marrow smear. This patient had a splenectomy and was discharged in good health. To date no complic ation has been detected. A brief review...
One Case of Hereditary Spherocytosis.
H J Jung, H S Cha, B H Ahn, Y H You, H S Lee
Clin Exp Pediatr. 1986;29(4):446-450.   Published online April 30, 1986
One cases of hereditary spherocytosis in a 3-month-old male baby was presented. Abnormal physical findings were anemia, jaundice 技 hepatosplenomegaly. Diagnosis were based on physical finding, presence of spherocytes in peripheral blood smear, bone marrow examination and osmotic fragility test. A brief review of related literature was made.
One Case of Hereditary Spherocytosis.
J S Hwang, Y D Lee, Y H Chung
Clin Exp Pediatr. 1984;27(11):1108-1112.   Published online November 30, 1984
One case of hereditary spherocytosis was presented. Diagnosis was based on7physical find- ings, spherocytes in peripheral blood, bone marrow, osmotic fragility test and autohemolysis test. A brief review of related literatures was also made.
A Case of Hereditary Spherocytosis.
Eui Lim Choi, Chul Hwan Park, Tae Gyu Hwang, In Soon Park, Soon Yong Lee
Clin Exp Pediatr. 1983;26(11):1120-1124.   Published online November 30, 1983
We observed a case of hereditary spherocytosis who was a 4-month-old boy with the chief complaints of jaundice and pallor. Evidence of the same disease was also found in the patient` s father who had never been symptomatic. Diagnosis was made by presence of spherocytes in peripheral blood smear, osmotic fragility- test and autohemolysis test. A brief review of literatures was made.
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