1.Lethal Measles Pneumonia after Allogenic Hematopoietic Stem Cell Transplantation.
Chang Nyol PAIK ; Dong Gun LEE ; Hyun Wha JUNG ; Jung Hyun CHOI ; Yu Kyung CHO ; Hoon Jun PARK ; Seung Hoon LEE ; Yoon Hee PARK ; Kyo Young LEE ; Wan Sik SHIN ; Woo Sung MIN ; Chun Choo KIM
Korean Journal of Infectious Diseases 2001;33(4):305-309
As a result of the enlarging pool of unvaccinated children and young adults, there has been an increase in measles in our countries. In these situation, it has been reported that measles associated pneumoinia is easily complicated with fatal respiratory failure, especially in immunocompromised patients. Herein we report the case of lethal measles pneumonia after allogenic hematopoietic stem cell transplantation in adults proven by autopsy. Recently, one case of measles was encountered in a 39-year-old female patients after allogenic bone marrow transplanted case (chronic myelogenous leukemia), who progressed into interstitial pneumonia pattern, despite treatment including antibiotics, immunoglobulin. The patient died of giant cell pneumonia compatible with that of measles which was comfirmed in the section of necropsy lung specimen.
Adult
;
Anti-Bacterial Agents
;
Autopsy
;
Bone Marrow
;
Bone Marrow Transplantation
;
Child
;
Female
;
Giant Cells
;
Hematopoietic Stem Cell Transplantation*
;
Hematopoietic Stem Cells*
;
Humans
;
Immunocompromised Host
;
Immunoglobulins
;
Lung
;
Lung Diseases, Interstitial
;
Measles*
;
Pneumonia*
;
Respiratory Insufficiency
;
Young Adult
2.A Case of Plasmodium falciparum Gametocytemia Successfully Treated with Primaquine.
In Bum SUH ; Do Kyung YOON ; Chae Seung LIM
Korean Journal of Infectious Diseases 2001;33(4):302-304
We experienced a case of Plasmodium falciparum gametocytemia successfully treated with primaquine in a twenty seven-years old woman. The patient had been admitted due to general malaise after diagosis and treatment of P. falciparum at Tanzania one month ago. On microscopic examination, P. falciparum gametocytemia was seen and treated with mefloquine for one week but gametocytemia was not disappeared. After primaquine treatment for two weeks, she was successfully treated.
Female
;
Humans
;
Mefloquine
;
Plasmodium falciparum*
;
Plasmodium*
;
Primaquine*
;
Tanzania
3.A Case of Cryptococcal Spondylitis Following Allogeneic Hematopoietic Stem Cell Transplantation.
Yoon Ho KO ; Dong Jun LIM ; Seong Su LEE ; Yu Kyung CHO ; Dong Gun LEE ; Jung Hyun CHOI ; Yoo Jin KIM ; Chang Ki MIN ; Dong Wook KIM ; Jeong Mi PARK ; Chun Choo KIM ; Wan Shik SHIN
Korean Journal of Infectious Diseases 2001;33(4):298-301
Skeletal cryptococcosis is an uncommon infection. Cryptococcus is a common cause of meningitis and infects 7~10% of patients with AIDS. As well as AIDS, the infection may be seen in association with leukemia, lymphoma, Hodgkin's disease, sarcoidosis, tuberculosis and diabetes, also in patients on steroid medication. But there is no case report of skeletal cryptococcosis following allogeneic hematopoietic stem cell transplantation. A 40-year-old woman was admitted to the hospital because of low back pain. She had chronic myelogenous leukemia for 2 years and underwent allogeneic hematopoietic stem cell transplantation 8 months ago. She have been treated with steroid and cyclosporine orally because of chronic graft versus host disease. On examination she was afebrile and had posterior lower lumbar tenderness. But, she had no reduced strength of low extremities. Open biopsy was underwent. Histology demonstrated budding, round-to-oval, refractile yeast-like organisms within debris. The results of a lumbar puncture were unremarkable and cerebrospinal fluid culture failed to grow bacteria and yeast. The patient was treated with amphotericin B (1 gram) and AmBisome (2.8 gram) over 6 weeks. Three months after cessation of therapy, the patient was doing well.
Adult
;
Amphotericin B
;
Bacteria
;
Biopsy
;
Bone Marrow Transplantation
;
Cerebrospinal Fluid
;
Cryptococcosis
;
Cryptococcus
;
Cyclosporine
;
Extremities
;
Female
;
Graft vs Host Disease
;
Hematopoietic Stem Cell Transplantation*
;
Hematopoietic Stem Cells*
;
Hodgkin Disease
;
Humans
;
Leukemia
;
Leukemia, Myelogenous, Chronic, BCR-ABL Positive
;
Low Back Pain
;
Meningitis
;
Sarcoidosis
;
Spinal Puncture
;
Spondylitis*
;
Tuberculosis
;
Yeasts
4.Cell Wall Proteins of Staphylococcus aureus Responsive to Oxygen Tension and Iron Concentration.
Seung Il LEE ; Yong LIM ; Sung Heui SHIN
Korean Journal of Infectious Diseases 2001;33(4):292-297
BACKGROUND: We previously reported that activity of iron-uptake systems (IUS) influenced on the growth of Staphylococcus aureus in laboratory medium and body fluids according to the iron and oxygen concentrations, which they are closely related each other in several microbial metabolism. In the present study, we tried to investigate the profiles of cell wall proteins of S. aureus according to the change of iron and oxygen concentrations. METHODS: SR-1 strain, whose IUS are defective, was isolated from the standard strain ATCC 6538 by repeated exposure against streptonigrin. These two strains were cultured under the aerobic, microaerobic and anaerobic conditions in the iron-sufficient BHI and iron-depleted BHI, respectively. Cell wall proteins were visualized by Coomassie staining after SDS-PAGE. RESULTS: Cell wall proteins of the both strains were expressed more than under the aerobic condition than under the anaerobic condition in the iron-sufficient medium as well as in the iron-deficient medium. However, expression of cell wall proteins of SR-1 strain was markedly inhibited compared to that of parental ATCC 6538 strain, especially in the iron-deficient medium. Among the proteins more expressed under the aerobic culture condition in the iron-deficient medium, about 88, 55, 39, 36, 35 and 33 kDa of proteins were iron-repressible and oxygen-inducible, and corresponded to the iron-repressible proteins which other researchers reported. CONCLUSION: Expression of cell wall proteins of S. aureus was affected by simultaneous and respective change of iron and oxygen concentrations. Activity of IUS influenced more on the expression of cell wall proteins of S. aureus in the iron-deficient environment than in the iron-sufficient environment. These results suggest the possibility that the iron-repressible and oxygen-inducible proteins mimic those (antigens) found commonly in clinical infections.
Body Fluids
;
Cell Wall*
;
Electrophoresis, Polyacrylamide Gel
;
Humans
;
Iron*
;
Metabolism
;
Oxygen*
;
Parents
;
Staphylococcus aureus*
;
Staphylococcus*
;
Streptonigrin
5.Evaluating the Necessity of Routine Monitoring of Netilmicin Serum Concentrations in Korean Pediatric Patients with Normal Renal Function.
Yun Ji CHOI ; Dong Il LEE ; Hong Bae KIM ; Yun Ju PARK ; Charles D SANDS
Korean Journal of Infectious Diseases 2001;33(4):285-291
BACKGROUND: When pediatric patients with normal renal function were given the recommended keep-up amount of aminoglicocide for the use, they showed a better clinical symptom not indicating the poisonous without checking serum concentrations. We studied this subject against the patients who used Netimilcin in order to know if the blood creatinine significantly increases in a clinic and if it reaches the maximum and minimum concentrations without adjusting the amount and the symptom of infection and the result get better. METHODS: We picked the maximum concentration of drugstuffs 30 minutes after injection and its minimum just prior to the next injection within 24~32 hours with a vein injection of 2 mg/kg/dose Netilmicin with the 8 hours difference against 16 patients at the age between 3 months and 14 years. We measured the blood creatinine at the beginning of the treatment and at the closing, and we decided the medicine serum concentration with TDX system and we counted the result of Pharmaco-kinetic parameter with Simkin PC clinical Database system. To check the patients' result of better clinical conditions, leukocyte values and the temperature were measured 72 hours after the treatment. The analysis of statistics was performed with the use of paired t-test. RESULTS: The average age of 16 patients shows 3.5+/-3.2, average weight 15.2+/-8.5 kg, the leukocyte value first 14.9+/-6.6X10X10X10/mm3, and 72 hours after the treatment it shows 6.6+/-1.9X10X10X10/mm3, average temperature fell from 37.7+/-1 celsius into 36.3+/-0.4 celsius. The average drug amount taken in case of patients showed 2.06+/-0.4, the average treatment period was 7.6+/-2.3 days, the maximum serum concentration shows 5.5+/-1.1 mg/mL, the minimum concentration shows 0.5+/-0.3 mg/mL. The average blood creatinine was first 0.52+/-0.19 mg/mL, and at closing 0.46+/-0.11 mg/dL (P=0.209). The minimum concentration didn't show more than 2 mcg/mL, the blood creatinine didn't increase showing 0.5 mg/mL(P=0.201). CONCLUSION: At the result of checking the medicine concentration of Netilmicin in pediatric patients in our clinic, there is no detecting the betterment of the clinical symptom owing to the decrease of the values of leukocyte. There was no necessity to adjust the amount of medicine from the beginning to the end as there was no sign of change of blood creatinine. In view of this result, we can understand that we don't need the regular examination of the medicine concentration about the aminoglicocide from Korean pediatric patients with normal renal function.
Creatinine
;
Humans
;
Leukocytes
;
Netilmicin*
;
Pediatrics
;
Veins
6.Status of Vivax Malaria in the Republic of Korea in 2000.
Jae Won PARK ; Young A KIM ; Joon Sup YEOM ; Jeong Sik YOO ; Byung Guk YANG ; Jong Yil CHAI
Korean Journal of Infectious Diseases 2001;33(4):280-284
BACKGROUND: Since 1997, the annual case occurrence of vivax malaria in the Republic of Korea have exceeded 1,000 cases since 1997. The military is thought to be an important source of the current outbreak. We collected various informations about malaria cases (soldiers, veterans and civilians) which occurred in 2000, and analyzed the characteristics of the current outbreak. METHODS: Informations about malaria cases of soldiers, veterans and civilians, including name, age, sex, day of onset, region, etc., were collected through the National Institute of Health. RESULTS: Out of total 4,141 cases, 1,288 (31.1%) occurred in the military, 1,273 (30.7%) occurred among the veterans, and 1,580 (38.2%) occurred among civilians. The monthly case occurrence reached its peak in early August. Areas such as Cheolwon, Yeoncheon and Paju showed the highest prevalence. CONCLUSION: It is considered that the current malaria outbreak has escaped from the exponential growth phase, however, more attention should be paid to prevent further spreading of malaria infection.
Humans
;
Malaria
;
Malaria, Vivax*
;
Military Personnel
;
Prevalence
;
Republic of Korea*
;
United Nations
;
Veterans
7.Pneumocystis carinii Pneumonia Following Stem Cell Transplantation.
Ji Hyeon JU ; Jung Hyun CHOI ; Dong Gun LEE ; Ji Yeon BAEK ; Yun Ho KOH ; Hae Jung LEE ; Se Hee KIM ; Ho Jin SHIN ; Yoo Jin KIM ; Yoon Hee PARK ; Chi Young PARK ; Wan Shik SHIN ; Chun Choo KIM
Korean Journal of Infectious Diseases 2001;33(4):273-279
BACKGROUND: Pneumocytitis cainii pneumonia (PCP) can occur in immunocompromised hosts especially such as AIDS or cancer patients. Although recent research had focused on PCP in AIDS patients, few studies have described the clinical presentations of PCP in recipients of stem cell transplantation (SCT). We evaluated the clinical manifestations of PCP in SCT patients admitted at St. Mary's hospital, Seoul, Korea. METHODS: The medical records of 17 PCP patients undergoing SCT between Feb. 1998 and Feb. 2000 were reviewed. The diagnosis of PCP was confirmed through the demonstration of Pneumocystis carinii via either cytology of brochoalveolar lavage (BAL) or histological technique of lung biopsy. CMV disease and CMV infection were confirmed by BAL culture and antigenemia respectively. RESULTS: Seventeen patients were all recipients of allogeneic SCT and 7 of 17 patients were performed non-sibling SCT. Patients presented with symptoms including brief period (4~23 days) of fever (76%), dyspnea (70%), cough (64%), and signs such as rale (58.8%). Sixteen patients (94%) had been receiving immunosuppressive agent such as cyclosporine A (64%) or FK506 (35%) without PCP prophylaxis. Eleven patients (64%) were treated with corticosteroid with mean dose of 16 mg/day prednisolone and mean duration of 4.6 months after post-SCT period. Twelve patients were co-infected with CMV. Another co-infected microorganisms were Pseudomonas aeruginosa, Mycobacterium tuberculosis, herpes simplex virus, parainfluenza virus. Average duration of treatment with trimethoprim-sulfamethoxazole (TMP/SMX) was 21+/-9 days. Four patients died, and three of them were related with PCP. CONCLUSION: PCP developed frequently in patients who were taking immunosuppressive drug due to graft versus host disease or were not taking TMP/SMX prophylaxis. High risk patients showing fever, cough, or dyspnea should be considered to take early bronchoscopic intervention for detection of PCP. When treat for PCP, it also be considered to the possibility of co- infection such as CMV.
Biopsy
;
Cough
;
Cyclosporine
;
Cytomegalovirus
;
Diagnosis
;
Dyspnea
;
Fever
;
Graft vs Host Disease
;
Histological Techniques
;
Humans
;
Immunocompromised Host
;
Korea
;
Lung
;
Medical Records
;
Mycobacterium tuberculosis
;
Paramyxoviridae Infections
;
Pneumocystis carinii*
;
Pneumocystis*
;
Pneumonia
;
Pneumonia, Pneumocystis*
;
Prednisolone
;
Pseudomonas aeruginosa
;
Respiratory Sounds
;
Seoul
;
Simplexvirus
;
Stem Cell Transplantation*
;
Stem Cells*
;
Tacrolimus
;
Therapeutic Irrigation
;
Trimethoprim, Sulfamethoxazole Drug Combination
8.Comparison of OptiMAL Test with GENEDIA Malaria (P.vivax) Ab Rapid I, II for Diagnosis of Plasmodium vivax in South Korean Soldiers.
Duck CHO ; Jae Gyun LIM ; Sang Oh LEE ; Byung Jo SO ; Chae Seung LIM ; Dong Wook RYANG
Korean Journal of Infectious Diseases 2001;33(4):267-272
BACKGROUND: The diagnosis of malaria has been usually made using microscopic examination of Wright stained thin blood films in Korean army. This method is labor-intensive, time consuming and requires the microscopic expertise. Therefore, the alternative techniques, rapid diagnostic test, have been sought for use in Korean army. We performed a comparison of the OptiMAL test with GENEDIA Malaria (P. vivax) Ab Rapid I, II to assess its sensitivity and specificity of Plasmodium vivax malaria. METHODS: Blood specimen were collected from 51 patients who were presented and initially diagnosed for P. vivax by the microscopy of blood smears and from 30 control patients without malaria infection at the Capital Armed Forces General Hospital (CAFGH) between October 2000 and February 2001. Among the 51 patients, we also collected 24 samples from 24 patients at 2 or 3 days after therapy. The OptiMAL test and GENEDIA Malaria (P. vivax) Ab Rapid I, II were performed according to the manufacturer's instructions on all samples respectively. RESULTS: Compared with the blood film, sensitivities and specificities of the OptiMAL test, GENEDIA Malaria (P. vivax) Ab Rapid I and GENEDIA Malaria (P. vivax) Ab Rapid II were 94.1~100% (29/29), 80.4~83.3%, 96.1~96.7% respectively. One case was interpreted as 'undetermined' by OptiMAL test. In 24 patients during therapy, the sensitivities of the OptiMAL test, GENEDIA Malaria (P. vivax) Ab Rapid I and GENEDIA Malaria (P. vivax) Ab Rapid II on 8 specimens with mean 120/microliter parasitemia and 16 specimens with negative parasitemia were 75~43.8%, 87.5~81.3%, 100~100% respectively. CONCLUSION: Our data demonstrated that the sensitivity and specificity of the GENEDIA Malaria (P. vivax) Ab Rapid I were not satisfactory, but the sensitivity and specificity of the OptiMAL test and GENEDIA Malaria (P. vivax) Ab Rapid II were relatively high and useful diagnostic tests for diagnosis of P. vivax in areas like the militaries where laboratory facilities are poor or non-existent.
Arm
;
Diagnosis*
;
Diagnostic Tests, Routine
;
Hospitals, General
;
Humans
;
Malaria*
;
Malaria, Vivax
;
Microscopy
;
Military Personnel*
;
Parasitemia
;
Plasmodium vivax*
;
Plasmodium*
;
Sensitivity and Specificity
9.Antimicrobial Susceptibilites of Glycopeptides, Arbekacin and Quinupristin/Dalfopristin against Staphylococcal aureus isolates.
Seung Hee HA ; Seok Hoon JEONG ; Tae Sik JEONG ; Dae Young SEO ; Chulhun CHANG ; Hee Jun NAM ; Young Woon BAEK ; Jong Heaon JI
Korean Journal of Infectious Diseases 2001;33(4):261-265
No abstract available.
Glycopeptides*
10.Antimicrobial Activities of Arbekacin against Clinical Isolates of Staphylococcus aureus and Coagulase-Negative Staphylococcus Species.
Seong Heon WIE ; Jin Han KANG ; Dong Ho HUH ; Dong Gun LEE ; Sang Il KIM ; Yang Ree KIM ; Jung Hyun CHOI ; Jong Hyun KIM ; Jin Hong YOO ; Jae Kyun HUR ; Wan Shik SHIN ; Moon Won KANG
Korean Journal of Infectious Diseases 2001;33(4):254-260
BACKGROUND: Most strains of methicillin-resistant Staphylococcus aureus (MRSA) now exhibit high-level resistance to various antibiotics, such as beta-lactam antibiotics, aminoglycosides, macrolides, tetracyclines and quinolones. Recent reports describing the therapeutic failure of vancomycin for MRSA infections have arisen considerable concerns regarding the emergence of MRSA strains, which will require new therapeutic agents. Arbekacin, an aminoglycoside antibiotic, has antibacterial activity against both gram-positive and gram-negative bacteria and is stable in the presence of aminoglycoside inactivating enzymes produced by S. aureus. In this study, we compared the antibacterial activity of arbekacin with those of vancomycin, gentamicin, and amikacin against Staphylococcus aureus (S. aureus) and coagulase-negative staphylococci (CNS). METHODS: For a collection of 549 S. aureus and 251 CNS isolates from three Catholic University Hospitals in Korea, minimum inhibitory concentrations (MICs) of arbekacin, vancomycin, amikacin and gentamicin were determined by agar dilution method using Mueller-Hinton agar according to NCCLS (National Committee for Clinical Laboratory Standards, USA) criteria. RESULTS: Among 549 S. aureus isolates, 278 isolates were MRSA and 271 isolates were methicillin- sensitive S. aureus (MSSA). MIC50 & MIC90 of arbekacin against 549 S. aureus were 0.5 & 1 microgram/mL, and MIC50 & MIC90 of vancomycin were 1 & 1 microgram/ mL. MIC of arbekacin against 549 S. aureus isolates ranges from 0.03 to 4 microgram/mL, and MIC of vancomycin against 549 S. aureus ranges from 0.25 to 2 microgram/ mL. MIC90 of amikacin against 549 S. aureus was 32 microgram/mL, and that of gentamicin was 128 microgram/mL. MICs of amikacin and gentamicin were variable, ranging from 0.125 to 256, and otherwise arbekacin and vancomycin revealed relatively narrow range of MICs. MIC90 of arbekacin against 278 MRSA isolates & 271 MSSA were 1 & 0.5 microgram/mL, and those of vancomycin against MRSA & MSSA were 1 & 1 microgram/mL. MIC90 of amikacin against 278 MRSA & 271 MSSA isolates were 32 & 4 microgram/mL, and that of gentamicin against MRSA & MSSA isolates were 128 & 32 microgram/ mL respectively. Among 251 CNS isolates, 122 isolates were MRCNS and 129 were MSCNS. MIC50 & MIC90 of arbekacin against 251 CNS isolates were 0.25 & 2 microgram/mL, and those of vancomycin were 1 & 2 microgram/mL. MIC of arbekacin against 251 CNS isolates ranges from 0.015 to 32 microgram/mL, and that of vancomycin isolates ranges from 0.25 to 2 microgram/mL. MIC90 of arbekacin against 122 MRCNS & 129 MSCNS isolates were 2 & 0.5 microgram/mL, and those of vancomycin were 2 & 2 microgram/mL. MIC90 of amikacin against 251 CNS isolates was 32 microgram/mL, and that of gentamicin was 128 microgram/mL for CNS. MIC90 of amikacin against 122 MRCNS & 129 MSCNS isolates were 128 & 8 microgram/mL, and those of gentamicin were 256 & 32 microgram/ mL. CONCLUSION: Considering above results, arbekacin can be a useful agent against most strains of MRSA and MRCNS, which exhibit high-level resistance to amikacin and gentamicin.
Agar
;
Amikacin
;
Aminoglycosides
;
Anti-Bacterial Agents
;
Gentamicins
;
Gram-Negative Bacteria
;
Hospitals, University
;
Korea
;
Macrolides
;
Methicillin-Resistant Staphylococcus aureus
;
Microbial Sensitivity Tests
;
Quinolones
;
Staphylococcus aureus*
;
Staphylococcus*
;
Tetracyclines
;
Vancomycin