1.A Case of Diabetes Insipidus in Patient with Sheehan's Syndrome
Hye Young PARK ; Moon Ho KANG ; Sung Gwang LEE ; Jung Ho YOUN ; Yeoung Sook KANG ; Deuk Jo KIM ; Yun Young CHOI ; Hee Young HWANG
Journal of Korean Society of Endocrinology 1996;11(1):108-113
Sheehans syndrome is a known complication of pregnancy, It was described as a syndrome of hypopituitarysm due to acute ischemic necrosis of the anterior pituitary gland secondary to severe postpartum bleeding and shock. The neurophysis is usually preserved. But it can be involved in severe cases manifesting as diabetes insipidus. Because of its rare coexistence with Sheehans syndrome, diabetes insipidus is seldom recognized as a potential postpartum complication. The report describes a patient who developed Sheehans syndrome and diabetes insipidus immediately following delivery. Diabetes insipidus resolved spontaneously after 15 months, while panhypopituitarysm is persistent.
Diabetes Insipidus
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Hemorrhage
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Humans
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Hypopituitarism
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Necrosis
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Pituitary Gland, Anterior
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Postpartum Hemorrhage
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Postpartum Period
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Pregnancy
;
Shock
2.Effect of Cytosine Arabinoside and Daunorubicin (AD) Combination Chemotherapy in Acute Myelogenous Leukemia.
Yeoung Sook KANG ; Hyun Sik JEONG ; Tae Seok KIM ; Hyun Seon YUN ; Deuk Jo KIM ; Jeong Ho YUN ; Seong Goyng LEE ; Hyeon Gyoo JI ; Gui Hyun HAM ; Jae Hoon LEE ; Dong Bok SHIN
Journal of the Korean Cancer Association 1997;29(1):160-170
PURPOSE: Important advances in the treatment of acute myelogenous leukemia have been made with the introduction of cytosine arabinoside (ara-C) and anthracyclines (daunorubicin) over the past 20 years. Currently, 60 to 80% of patients with acute myelogenous leukemia achieve complete remission with induction chemotherapy consisting of ara-C and daunorubicin (adriamycin) AD ("7+3"). The one-fourth of complete responders will have extended long-term survival and may be cured. Therefore wetreated patients with acute myelogenous leukemia admitted to our hospital with AD ("7+3") regimen. METHODS: Induction therapy; Thirty four patients with previously untreated acute myelogenous leukemia received AD ("7+3") regimen (ara-C, 200 mg/m2/d by continuous infusion for seven days, and daunorubicin, 45 mg/m2/d for 3 days). The second course of therapy was AD ("5+2"), if the patients failed to enter remission. Consolidation therapy; three cycles of consolidation chemotherapy were administered with at least 4 week interval following remission. Course 1; ara-C at 100 mg/m2 by subcutaneous injection every 12 hour for seven days, 6-thioguanine at every 12 hour 100 mg/m2 orally every 12 hour for 7 days). Course 2; ara-C (same as course 1) at 100 mg/m2 by subcutaneous injection every 12 hour for seven days, vincristine at 1.5 mg/m2 (maximum 2 mg) by bolus injection for 1 day, prednisolone at 40 mg/m2 (maximum 60 mg) orally for 7 days. Course 3; ara-C (same as course 1) daunorubicin at 45 mg/m2 by 1 hour infusion for 3 dyas. RESULTS: Sixty-eight percent of the 34 patients entered complete remission. The remission duration for all patients in complete remission ranged from 4 weeks to 3122+ weeks, with the median of 50 weeks. The median duration of survival in complete responder group was 62 weeks. Twenty-Six percent of patients with complete remission are alive at 5 years. Cases with extramedullary leukemic involvement were found in four patients; M2 with orbital mass, M3 and M4 with CNS leukemia, M5a with subcutaneous nodules. Among the potential prognostic variables including age, initial WBC count, percent of blast in peripheral blood,none was statistically related to prognosis. CONCLUSION: Combination chemotherapy with cytosine arabinoside and daunorubicin is a effective regimen for acute myelogenous leukemia as much as other regimen. Futher clinical trials for effective treatment regimen and method are necessary to raise the complete remission rate.
Anthracyclines
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Consolidation Chemotherapy
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Cytarabine*
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Cytosine*
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Daunorubicin*
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Drug Therapy
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Drug Therapy, Combination*
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Humans
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Induction Chemotherapy
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Injections, Subcutaneous
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Leukemia
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Leukemia, Myeloid, Acute*
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Orbit
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Prednisolone
;
Prognosis
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Thioguanine
;
Vincristine