1.Clinical Experience of Plasma Exchange.
Korean Journal of Blood Transfusion 1995;6(2):131-140
BACKGROUND: Plasmapheresis or plasma exchange is the procedure to remove various pathogenic materials from the circulation of patients and retransfuse the formed elements into the doners with type specific fresh frozen plasma or albumin for the replacement of the withdrawn plasma. METHODS: In order to evaluate clinical experience of plasma exchange, we examined a total of 133 plasma exchange procedure on 25 patients of January 1993 - May 1994 in Kyungpook national university hospital. RESULTS: The results are as follows: 1. There were 8 kinds of diseases and the most frequent diseases was Guillian-Barre syndrome(l 2 cases) and the decreasing order was CIDP(6 cases), multiple myeloma(2 cases), acute fulminant hepatitis(1 case), mushroom poisoning(1 case), lupus nephritis(l case), TTP(I case) and myasthenia gravis(l case). 2. The patient's age ranged from 13 to 65 years. 3. There were 14 males and 11 females and the sex ratio was 1.3:1. 4. We had got clinical improvement in 16 of 25 cases, especially most dramatic effect in Guillian-Barre syndrome. CONCLUSION: To achieve more successful outcome of plasma exchange, we should select patients with restrict application, prevent rebound phenomenon with intense practice, choose what kind of replacement fluid to consider patient's clinical condition and check serological parameter with clinical evaluation to monitor effectiveness of treatment.
Agaricales
;
Female
;
Gyeongsangbuk-do
;
Humans
;
Male
;
Plasma Exchange*
;
Plasma*
;
Plasmapheresis
;
Sex Ratio
2.Platelet counts and size in normal pregnancy and pregnancy with preeclamsia or IUGR.
Hye Kyung KIM ; Eui Sik JUNG ; Hye Sung PARK ; Ok Kyung SON ; Chang Suh PARK ; Chang Yong PARK ; In Suh PARK
Korean Journal of Obstetrics and Gynecology 1993;36(7):3055-3061
No abstract available.
Blood Platelets*
;
Fetal Growth Retardation*
;
Platelet Count*
;
Pregnancy*
3.Dysembryoplastic Neuroepithelial Tumors in Children with Intractable Seizures: Report of Two Cases.
Mun Hyang LEE ; Seung Chyul HONG ; Yeon Lim SUH ; Hye Kyung YOON ; Bo Kyung KIM
Journal of the Korean Child Neurology Society 1998;5(2):334-341
We report 2 cases of pediatric DNTs which presented with intractable seizures and no other associated neurologic abnormalities. They showed typical appearance of DNTs on neuroimaging and histopathology. Most patients with DNT can be cured by surgical treatment with exellent outcome and do not need ratio- or chemotheraphy. This study indicates that it is quite important to consider DNTs as one of differential diagnoses in patients with intractable seizures especially when they present only with seizures without other neurologic symptoms.
Child*
;
Diagnosis, Differential
;
Humans
;
Neoplasms, Neuroepithelial*
;
Neuroimaging
;
Neurologic Manifestations
;
Seizures*
4.Ectopic paragonimiasis on colon wall and mesocolon of the descending colon
Hae Jeong JEON ; Kyung Chun HONG ; Hye Kyung CHUNG ; Won Hyuck SUH
Journal of the Korean Radiological Society 1983;19(2):426-429
Paragonimiasis is prevalent in Far East and a kind of endemic Korean disases. The primary site of humanparagonimiasis is the lung, but hte ectopic infection of lung fluke has been reported by many authors. Weexperienced one case of abdominal paragonimiasis in a 44 year old male with a complaint of left lowerquadrantpain. Physical examination, barium enema, and other data suggested the possibility of tumor originating from thewall of descending colon. (intramural tumor). Postoperative specimen taken from the solid tumorous lesion showedparasitic granuloma, characteristic of Paragonimus Westermani. Here, we report a case of very peculiar ectopicparagonimaisis involved descending colon wall simulating neoplastic tumor, and also review the literaturesbriefly.
Barium
;
Colon
;
Colon, Descending
;
Enema
;
Far East
;
Granuloma
;
Humans
;
Lung
;
Male
;
Mesocolon
;
Paragonimiasis
;
Paragonimus westermani
;
Physical Examination
;
Trematoda
5.Three cases of potter syndrome.
Kyung Won JUNG ; Hye Sung PARK ; Chang Suh PARK ; Chan Yong PARK ; Sung Jin CHO ; In Suh PARK
Korean Journal of Perinatology 1993;4(2):247-255
No abstract available.
6.Surgical treatment of severe generalized idiopathic gingival fibromatosis on mandible and maxilla:report of a case.
Yong Oh LEE ; Seon Hye MOON ; Hye Kyung SUH ; Hee Suck JANG ; Gong Uck SA ; No Bu PARK
Journal of the Korean Association of Oral and Maxillofacial Surgeons 1993;19(1):37-43
No abstract available.
Fibromatosis, Gingival*
;
Mandible*
7.Surgical treatment of severe generalized idiopathic gingival fibromatosis on mandible and maxilla:report of a case.
Yong Oh LEE ; Seon Hye MOON ; Hye Kyung SUH ; Hee Suck JANG ; Gong Uck SA ; No Bu PARK
Journal of the Korean Association of Oral and Maxillofacial Surgeons 1993;19(1):37-43
No abstract available.
Fibromatosis, Gingival*
;
Mandible*
8.Correlation between Nuclear Grades and the Numbers of AgNORs and PCNA Labeling Indices in Renal Cell Carcinoma.
Hye Jin LEE ; Young Im HAN ; Kang Suek SUH ; Sun Kyung LEE
Korean Journal of Pathology 1996;30(2):132-139
The author examined the number of AgNORs and PCNA labeling indices by histochemical and immunohistochemical studies in 20 cases of renal cell carcinoma, composed of 5 cases according to the nuclear grades. The results obtained are summarized as follows; 1) Mean number of AgNORs according to the nuclear grades of renal cell carcinoma were 1.38+/-0.40 (mean+/-standard deviation) for Grade I, 2.53+/-0.33 for Grade II, 5.43+/-0.66 for Grade III, and 7.88+/-0.72 for Grade IV. The mean numbers of AgNORs according to the nuclear grades were significantly increased(p=0.0005). 2) PCNA labeling indices (positive nuclear ratio) according to the nuclear grades of renal cell carcinoma were 5.90+/-2.36 for Grade I, 19.30+/-6.71 for Grade II, 45.73+/-8.62 for Grade III, and 61.83+/-6.34 for Grade IV. Also, the PCNA labeling indices according to the nuclear grades were significantly increased(p=0.0008). 3) The mean numbers of AgNORs directly correlated with the PCNA labeling indices (r=0.9861, p<0.001). On the basis of the above results, it was considered that the numbers of AgNORs and PCNA labeling indices as markers of proliferative activity of tumor cells correlate well with the nuclear grades of renal cell carcinoma.
9.Malignant Small Cell Tumor of the Thoracopulmonary Region (Askin Tumor): Report of a case.
Young Im HAN ; Hye Jin LEE ; Kang Suek SUH ; Sun Kyung LEE
Korean Journal of Pathology 1995;29(5):687-690
Malignant small cell tumor(MSCT) of the thoracopulmonary region(Askin tumor) is extremely rare and is seen predominantly in children and adolescents. This tumor represents a distinct clinicopathologic entity of neuroectodertnal origin, arising from the soft tissues of the chest wall or peripheral lung. This tumor tends to recur locally, but does not seem to disseminate widely. The overall survival is poor. Recently, we experienced a case of the MSCT of the thoracopulmonary region of a 12-year-old female. She was admitted because of a chest wall mass on radiographic examination, and a complaint of intermittent chest pain. Grossly, the mass was lobulated, round and had a solid appearance with focal necrosis and hemorrhage on the cut surface. Histologically, small round to oval cells were arranged in compact sheets, nests and lobular patterns with intervening fibrovascular stroma. Ultrastructurally, the presence of loose-fitting membrane-bound neurosecretory granules was noted.
Child
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Adolescent
;
Male
;
Female
;
Humans
10.Sertoli-Leydig Cell Tumor of Hemangiopericytoma Pattern: A case report.
Hye Jin LEE ; Young im HAN ; Hyeon Ok KIM ; Kang Suek SUH ; Sun Kyung LEE
Korean Journal of Pathology 1995;29(6):815-818
The Sertoli-Leydig cell tumor is a gonadal tumor of sex-cord stromal type, similar to that seen in of the various phases of testicular development in the male. This tumor is exceedingly rare, accounting for only 0.1% to 0.5% of all primary ovarian neoplasms. It occurs predominantly in the second and third decades(mean age about 25 years), less than 10% after menopause. We investigated a case of poorly differentiated Sertoli-Leydig cell tumor of right ovary, occured in a 76-year-old woman. Grossly, the tumor measured 2, 100 gm in weight and 25 x 19 x 8 cm in dimensions. The outer surface was smooth and glistening without rupture of the capsule. Cut sections revealed a multilobulated brown solid mass with multiple cystic change. Microscopically, it showed the typical findings o a Sertoli-Leydig cell tumor. The characteristic feature is hemangiopericytoma paftem of sarcomatoid spindle cells. Therefore, we present it with a brief review of the literature.
Female
;
Humans