- An Overview and Future Perspective on Endocrine Disruptors.
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Chul Woo Lee, Kyung Hee Choi, Seok Won Jeong, Hye Lim Kim, Young Rok Seo
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J Korean Endocr Soc. 2009;24(1):7-14. Published online March 1, 2009
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DOI: https://doi.org/10.3803/jkes.2009.24.1.7
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Citations
Citations to this article as recorded by  - Safety Assessment of Endocrine Disruption by Menopausal Health Functional Ingredients
Soyeon Kang, Hagyeong Jo, Mee-Ran Kim
Healthcare.2021; 9(10): 1376. CrossRef - Prognostic Value of p53 and Cyclin D1 in Papillary Thyroid Carcinoma
Jae Yeon Seok, Dong Hae Chung, Yoo Seung Chung, Jung Won Ryu, Young Don Lee
Korean Journal of Endocrine Surgery.2015; 15(2): 25. CrossRef - Prognostic Value of p53 and Cyclin D1 in Papillary Thyroid Carcinoma
Jae Yeon Seok, Dong Hae Chung, Yoo Seung Chung, Jung Won Ryu, Young Don Lee
Korean Journal of Endocrine Surgery.2015; 15(2): 25. CrossRef - Tributyltin increases the expression of apoptosis- and adipogenesis-related genes in rat ovaries
Hyojin Lee, Sojeong Lim, Sujin Yun, Ayoung Yoon, Gayoung Park, Hyunwon Yang
Clinical and Experimental Reproductive Medicine.2012; 39(1): 15. CrossRef - Epigenetic control of endocrine disrupting chemicals on gynecological disease: Focused on phthalates
Hyun Hee Cho
Korean Journal of Obstetrics & Gynecology.2012; 55(9): 619. CrossRef
- A Case of Multiple Endocrine Neoplasia Type 1.
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Soon Jib Yoo, Bong Yun Cha, Kwang Woo Lee, Ho Young Son, Sung Koo Kang, Jong Man Won, Young Seok Cho, Yong Jik Sung, Kyung Sub Song, Jin Young Yoo, Chul Woo Lee
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J Korean Endocr Soc. 1997;12(1):111-119. Published online January 1, 2001
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Abstract
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- Multiple endocrine neoplasia type 1 (MEN 1) is the association of neoplastic transformation of parathyroid, pituitary, and pancreatic islet cells. This syndrome is inherited as an autosomal dominant trait. A 38-year-old woman presented with general weakness and mental changes. She had experienced same symptoms 7 years ago, after then her weight gradually increased. Insulinoma was suspected by markedly decreased blood glucose level (20mg/dL) and the increased insulin/glucose ratio (0.43) that sampled in emergency room at the time of mental change. Unusually large pancreatic tail mass and Lt, adrenal gland mass were detected by abdominal CT. Percutaneous transhepatic portal vein catheterization with insulin sampling showed sudden step up of insulin/glucose ratio at the middle portion of pancreas. Measuring of basal pituitary hormones as a screening procedure of MEN showed increased basal prolactin level. Combined pituitary stimulation test showed blunted response of prolactin to TRH and sellar magnetic resonance imaging showed intrasellar mass. Thyroid nodule was palpated on her anterior neck. Thyroid scintigram showed cold nodule, and there was no lymphadenopathy around the nodule by the thyroid sonogram. Fine needle aspiration cytology showed benign hyperplastic follicular cells only. Serum ionized calcium and parathyroid hormone level were normal. Under the impression of MEN type I, the distal pancreatectomy, splenectomy, Lt. thyroid lobectomy and Lt. adrenalectomy was performed at the same time. Histologic examination of the surgically removed tissues revealed pancreas islet cell tumor, adrenal cortical adenoma and thyroid adenoma. Transient hyperglycemia was developed after surgical intervention, but thereafter she never felt any symptoms of hypoglycemia till now and her blood glucose showed completely normal level with oral glucose tolerance tests. We present this case with a review of literature.
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