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RISS 인기검색어
- 검색키워드
- 저자 : 박문성(MS Park) (검색결과 5 건)
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박문성(MS Park) 대한산부인과학회 1976 Obstetrics & Gynecology Science Vol.19 No.11
저자는 난소 간질선의 기원을 검색할 목적으로 체중 8-10gm되는 마우스 암컷을 사용하여 양측난소를 절제하고 그중 좌측 난소를 자신의 비장내에 자가 이식한후 1일부터 19일까지 격일로 도살하여 조직 표본을 만들어 몇가지 특수 염색을 시행하였고 검경하여 다음과 같은 결론을 얻었다. 1. 난소 이식후 1일부터 괴사가 일어나며 5일부터 재생이 시작된다. 2. 재생된 난소채는 거의 완전한 상태로 재생된다. 3. 배란을 못하게 된 난포가 폐쇄난포로 변화되면서 난포막 세포가 공포화되고 이들 세포가 간질조직으로 유리되면서 간질선으로 이행된다. The interstitial cells of the human ovaries were began to appear in late fourth decade thereafter increased in number and were ascribed to hormonal secretion in menopaused woman and they were especially well developed in rodents and formed acinar structures in the them . And such interstitial glands in the rodents could be induced by administration of formalin as stressor and induced by auto transplantation of the ovary into the spleen of the spayed mice . And the regenerated ovarian tissue within the spleen had some amounts of mucosubstances Therefor the author try to search the histogenesis of interstitial glands within the autotransplanted ovaries into the spleen of spayed mice by various histochemical techniques. Pre-estrous mice were spayed, the left ovary were autotransplanted into the spleen and were kept for 1, 3, 5, 7, 9, 11, 13, 15, 17 and 19days Paraffine sections were made acoriding to routine histologic methods and several kinds of staining for mucosubstances and for collagen fibers were made the following were ensued. 1. The ovarian transplants were undergone necrotic changes 1 day after transplantation and began to regenerated 7 days after transplantation. 2. The degree of the regeneration within the ovarian transplants were almostly complete in degree. 3. during the change of the unrippened follicle into the atretic follicle, there were swelling of the theca cells and thosecells were released into the ovarian stroma and acinar structure i.e. interstitial glands.
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박문성(MS Park),고원균(WK Ko),황준석(JS Whang),이정우(JW Lee) 대한산부인과학회 1975 Obstetrics & Gynecology Science Vol.18 No.10
1) 정상분만을 한 36세의 경산부에서 산후 제 7일에 발생한 후복강출혈을 일으킨 례를 보고한다. 2) 문헌상으로 약 90여 예가 보고 되었고 사망률은 약 50%에 이른다. 3) 비록 드물게 있으나 진단이 어렵고 처치를 약간만 지연기켜도 사망할 수가 있으므로 세심한 관찰과 주의를 요한다. 4) 원인, 진단, 치료 및 사망률에 관하여 간단히 기술하였다. We have made a report of a patients who had a massive retroperationeal hemorrhage from the rupture of the utero-ovarian vessels. This is a serious and william by reviewing of the literature in 1904, reported 32 cases including a case of his own, approximately 90 cases have been reported . We present here another such case without having any apparent cause, which was treated with immediate surgical intervention and we have described this briefly.
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황혜경(HK Whang),박문성(MS Park),고원균(WK Ko),김영한(YH Kim) 대한산부인과학회 1974 Obstetrics & Gynecology Science Vol.17 No.1
1) 17세된 미혼여성의 외음부 및 회음부에 걸쳐 발생한 거대 첨규 콘디로마 1예의 절제 후 무게는 710mg 이었다. 2) 문헌상으로 이때까지 보고된 첨규 콘디로마 중 최대의 것으로 사료된다. 3) 첨규 콘디로마의 발생원인, 임상, 증상, 진단 및 치료방법에 대하여 문헌상으로 고찰하였 다. Condyloma accuminatum is not rare disorder but is rapidly growing tumor usually occuring on or near the anogenital region. Because of the typical gross appearance of the hyperplastic warty growth, the diagnosis is usually unmistakable. In regard to size we believe thid case is the largest one reported in medical literature. We reported this case because of its unusual size and clinical presentation.
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고원균(WK Ko),박문성(MS Park),황준석(JS Whang),김영한(YH Kim) 대한산부인과학회 1976 Obstetrics & Gynecology Science Vol.19 No.3
A large cyst attacted to right salpinx was found when an exploratory laparotomy was done on 26 year old patient who complained of a distended abdomen. Although the cyst was confirmed pathologically as a tuberculous tubal cyst, no similiar cases have been reported elsewhere as far as our information goes. We present this because of its rarity and unusual pathologic entity.
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알파태아단백 (α-fetoprotein) 치 상승을 보인 선천성 피부결손 (Aplasia cutis congenita) 1 예
김정선,박문성,오기석,양정인,김행수,한기수 대한산부인과학회 1998 Obstetrics & Gynecology Science Vol.41 No.3
저자들은 본원 산부인과에서 임신 중기 모체혈청 알파태아단백치와 양수내 알파태아단백치의 증가를 동반한 선천성 피부 결손증 태아를 분만한 산모를 경험하였기에 문헌고찰과 함께 보고하는 바이다. Aplasia cutis congenita is an extremely rare disease characterized by congenital localized or widespread absence of skin. We present a catastrophic case of aplasia cutis congenita from a pregnancy complicated by elevated maternal serum and amniotic fluid -fetoprotein levels with a brief review of literatures. Delivery occurred at 38 weeks by cesarean section due to larger fetal head. The neonate lacked more than 90% of his skin and died in soon.
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