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Klinefelter 증후군에 병발된 원발성 종격동 생식세포종
김용조 ( Yong Jo Kim ),권교선 ( Gyo Seon Kwun ),이영우 ( Young Wo Lee ),김경태 ( Kyung Tae Kim ),박연희 ( Yeon Hee Park ),류백렬 ( Baek Yeol Ryoo ),김태유 ( Tae You Kim ),임영혁 ( Young Hyuck Im ),이춘택 ( Choon Taek Lee ),강윤구 대한결핵 및 호흡기학회 1996 Tuberculosis and Respiratory Diseases Vol.43 No.6
천은미(Eun Mee Cheon),이가희(Ka Hee Lee),남현석(Hyeon Seok Nam),권교선(Gyo Seon Kwun),김형건(Hyung Gun Kim),유영진(Young Jin Yuh),이상구(Sang Goo Lee),손태용(Tae Yong Son),이진오(Jhin Oh Lee),강태웅(Tae Woong Kang) 대한내과학회 1995 대한내과학회지 Vol.49 No.3
Multiple endocrine neoplasia IIb is diagnosed when medullary thyroid carcinoma, pheochromocytoma and mucosal neuromas are associated, Other features of this syndrome include a marfsnoid habitus, pectus excurvatum and long, thin extremities. We found a patient with these features: medullary thyroid carcinoma pheochromocytoma, mucosal neuromas and marfanoid habitus. A 19-year old female patient was transferred to our department. for the evaluation of fluctuating blood pressure, facial flushing and abdominal pain after total thyroidectomy which revealed medullary thyroid carcinoma in the left lobe of her thyroid gland. She had long and thin extremities and marfanoid habitus. Multiple mucosal nodules were found on the tip of her tongue and pathologically confirmed as mucosal neuromas. 24 hours urine VMA and metanephrine were markedly elevated and bilateral adrenal masses were found on the abdominal CT, Bilateral adrenalectomy was performed after pretreament with phenoxybenzamine for 2 weeks, which confirmed pheochromocytoma. The screening tests of serum calcitonin for her family members were all within normal limits.
성주병(Ju Byeung Sung),김용조(Yong Cho Kim),권교선(Gyo Seon Kwun),장은정(Eun Jung Jang),류백렬(Baek Yeol Ryoo),김태유(Tae You Kim),임영혁(Young Hyuck Im),강윤구(Yoon Koo Kang),김창민(Chang Min Kim),이승숙(Seung Sook Lee),이진오(Jhin 대한내과학회 1997 대한내과학회지 Vol.53 No.4
Multiple primary malignant neoplasms (MPMN) are defined by the presence of multiple primary cancers of multicentric origin and/or different tissues. The incidence of MPMN is less than 1% in Korea and recently seems to be increased due to early detection of cancer and prolonged survival of cancer patients. Previous investigations suggest that non-Hodgkin's lymphoma (NHL) may be associated with chronic liver disease and hepatocellular carcinoma (HCC). The pathogenesis of this association is thought to be due to chronic antigenic stimulation, the presence of HBsAg, and immunosuppressive therapy. We report a case of synchronous NHL and HCC in a 54-year-old man which is thought to be associated with hepatitis B virus infection. Pathological examination and immunohistochemical study of neck lymph node and liver mass biopsies showed diffuse large cell lymphoma and HCC, respectively. He was treated initially with EPOCH (etoposide, vincristine, doxorubicin, cyclophosphamide and prednisolone) chemotherapy for NHL and transarterial chemoembolization with doxorubicin, mitomycin-c, lipiodol, and gelfoam for HCC.
전이성 분화 갑상선암에서 200mCi 방사성 옥소 치료효과 평가를 위한 혈청 Thyroglobulin 추적검사와 전신스캔의 의의
최창운(Chang Woon Choi),임상무(Sang Moo Lim),홍성운(Sung Woon Hong),윤종길(Jong Kil Yoon),이창희(Chang Hee Lee),정상훈(Sang Hoon Jeong),권교선(Gyo Seon Kwun) 대한핵의학회 1995 핵의학 분자영상 Vol.29 No.4
N/A Thirty-eight patients with metastatic well-differentiated thyroid carcinoma treated with 200mCi 131I were false negative serum thyroglobulin values during TSH suppression or at anti-thyroglobulin antibody(+) and discrepancies between findings of whole body scan and serum thyroglobulin level. After one to five cycles of 200mCi 131I therapy, complete remission and partial were achieved at 5.3% and 57.9%, respectively. We concluded that all of serum thyroglobulin, TSH, anti-thyroglobulin antibody, 131I or 123I whole body scan were necessary in follow up of metastatic well-differentiated thyroid carcinoma. Also, if there was no response after repetitive 200mCi 131I therapy, higher doses of 131I therapy should be considered.