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Pregnancy and Pheochromocytoma: A Dangerous Liaison 妊娠与嗜铬细胞瘤:危险的联系
Endocrinologist Pub Date : 2010-03-01 DOI: 10.1097/TEN.0B013E3181D4BF70
J. George, V. Sarathi, T. Bandgar, P. Menon, N. Shah
{"title":"Pregnancy and Pheochromocytoma: A Dangerous Liaison","authors":"J. George, V. Sarathi, T. Bandgar, P. Menon, N. Shah","doi":"10.1097/TEN.0B013E3181D4BF70","DOIUrl":"https://doi.org/10.1097/TEN.0B013E3181D4BF70","url":null,"abstract":"Abstract: Pheochromocytoma is rarely observed during pregnancy. The diagnosis is often overlooked for the more common pre-eclampsia. Maternal prognosis depends on early diagnosis and multidisciplinary management prior to tumor resection. The literature is replete with mistakes in diagnosing and managing this disease. We report 3 cases of pheochromocytoma during pregnancy each with varied presentation, management, and culmination.","PeriodicalId":50531,"journal":{"name":"Endocrinologist","volume":"1 1","pages":"58-59"},"PeriodicalIF":0.0,"publicationDate":"2010-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83075014","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
Three Case Reports of Neonatal Hyperthyroidism 新生儿甲状腺功能亢进3例报告
Endocrinologist Pub Date : 2010-03-01 DOI: 10.1097/TEN.0B013E3181D4AB73
Xiu-jing Wu, Li-hua Chen, Ya-ping Xu
{"title":"Three Case Reports of Neonatal Hyperthyroidism","authors":"Xiu-jing Wu, Li-hua Chen, Ya-ping Xu","doi":"10.1097/TEN.0B013E3181D4AB73","DOIUrl":"https://doi.org/10.1097/TEN.0B013E3181D4AB73","url":null,"abstract":"To emphasize the causes, clinical features, diagnosis, management, and prognosis of hyperthyroidism in newborns, 3 cases of neonatal hyperthyroidism were analyzed. The cases were all low birth weight babies, and 2 of them were premature, the other was a term infant. Their mothers' histories were all positive for Graves' disease. In all cases, the infants exhibited tachycardia on admission. Case 1 presented mainly as splenohepatomegalia, case 2 presented mainly as heart failure and pneumonedema, whereas case 3 presented as hepatitis syndrome. The test of thyroid function and history of the mother confirmed the diagnosis of hyperthyroidism. Antithyroid drug therapy was administrated for all 3 cases, 2 with propylthiouracil and 1 with tapazole. In cases 1 and 2, thyroid function recovered after 4 to 5 weeks of treatment, and persisted for the following 3 months. Case 3 recovered after 3 months of therapy, which might be associated with a delay of diagnosis and severe symptoms. Neonatal hyperthyroidism is a rare disorder and usually associated with maternal Graves' disease. Although most neonatal hyperthyroidism is temporary, it may affect many organ systems and cause developmental delay in infants. Early diagnosis and prompt treatment consisting of antithyroid drugs in conjunction with iodine, β-receptor blocking agents, and at times glucocorticoids and digoxin, are the key elements in management of this disease.","PeriodicalId":50531,"journal":{"name":"Endocrinologist","volume":"39 1","pages":"52-54"},"PeriodicalIF":0.0,"publicationDate":"2010-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74130233","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Neurofibromatosis Type I, Pheochromocytoma, Fibrous Osseous Dysplasia, and Osteoporosis: A Rare and Unusual Combination I型神经纤维瘤病、嗜铬细胞瘤、纤维性骨发育不良和骨质疏松症:罕见和不寻常的组合
Endocrinologist Pub Date : 2010-03-01 DOI: 10.1097/TEN.0B013E3181D5A2EF
A. Polymeris, Antonis Sykiotis, H. Karga
{"title":"Neurofibromatosis Type I, Pheochromocytoma, Fibrous Osseous Dysplasia, and Osteoporosis: A Rare and Unusual Combination","authors":"A. Polymeris, Antonis Sykiotis, H. Karga","doi":"10.1097/TEN.0B013E3181D5A2EF","DOIUrl":"https://doi.org/10.1097/TEN.0B013E3181D5A2EF","url":null,"abstract":"","PeriodicalId":50531,"journal":{"name":"Endocrinologist","volume":"60 2 1","pages":"75-77"},"PeriodicalIF":0.0,"publicationDate":"2010-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77657421","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Hypokalemic Periodic Paralysis in Hyperthyroidism–Rare Event: Case Presentation and Review of Literature 甲状腺机能亢进患者低钾血症性周期性麻痹——罕见事件:病例报告及文献回顾
Endocrinologist Pub Date : 2010-03-01 DOI: 10.1097/TEN.0B013E3181D59AB3
D. Radulescu, A. Pârv, S. Pripon, M. Rădulescu, I. Gulei, A. Buzoianu
{"title":"Hypokalemic Periodic Paralysis in Hyperthyroidism–Rare Event: Case Presentation and Review of Literature","authors":"D. Radulescu, A. Pârv, S. Pripon, M. Rădulescu, I. Gulei, A. Buzoianu","doi":"10.1097/TEN.0B013E3181D59AB3","DOIUrl":"https://doi.org/10.1097/TEN.0B013E3181D59AB3","url":null,"abstract":"","PeriodicalId":50531,"journal":{"name":"Endocrinologist","volume":"269 1","pages":"72-74"},"PeriodicalIF":0.0,"publicationDate":"2010-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"87077874","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
Congenital Adrenal Hyperplasia With Normal Pregnancy Outcome: A Case Report With Review of Literature 先天性肾上腺增生伴正常妊娠结局:1例报告并文献复习
Endocrinologist Pub Date : 2010-03-01 DOI: 10.1097/TEN.0B013E3181CB47EB
S. Acharya, R. Gopal, P. Menon, T. Bandgar, N. Shah
{"title":"Congenital Adrenal Hyperplasia With Normal Pregnancy Outcome: A Case Report With Review of Literature","authors":"S. Acharya, R. Gopal, P. Menon, T. Bandgar, N. Shah","doi":"10.1097/TEN.0B013E3181CB47EB","DOIUrl":"https://doi.org/10.1097/TEN.0B013E3181CB47EB","url":null,"abstract":"","PeriodicalId":50531,"journal":{"name":"Endocrinologist","volume":"11 1","pages":"46-47"},"PeriodicalIF":0.0,"publicationDate":"2010-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"75743498","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Parathyroid Carcinoma, a Rare Cause of Hypercalcemia in a Patient With B-Cell Non-Hodgkinʼs Lymphoma 甲状旁腺癌是b细胞非霍奇金淋巴瘤患者高钙血症的罕见病因
Endocrinologist Pub Date : 2010-03-01 DOI: 10.1097/TEN.0B013E3181D4AC25
M. Halenka, Natalie Klusova, P. Koranda, L. Kučerová, D. Karásek, Z. Fryšák
{"title":"Parathyroid Carcinoma, a Rare Cause of Hypercalcemia in a Patient With B-Cell Non-Hodgkinʼs Lymphoma","authors":"M. Halenka, Natalie Klusova, P. Koranda, L. Kučerová, D. Karásek, Z. Fryšák","doi":"10.1097/TEN.0B013E3181D4AC25","DOIUrl":"https://doi.org/10.1097/TEN.0B013E3181D4AC25","url":null,"abstract":"","PeriodicalId":50531,"journal":{"name":"Endocrinologist","volume":"4 1","pages":"86-89"},"PeriodicalIF":0.0,"publicationDate":"2010-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85932731","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Case of Extra-Adrenal Paraganglioma Localized in Retroperitoneum Diagnosed With FDG-PET: Case Report and Review of the Literature FDG-PET诊断腹膜后肾上腺外副神经节瘤1例:病例报告及文献复习
Endocrinologist Pub Date : 2010-03-01 DOI: 10.1097/TEN.0B013E3181D4BF84
B. Ozturk, U. Coşkun, E. Yaman, O. Akdemir, A. Çakır, L. Memış, K. Sezer, A. Kaya, R. Yıldız, U. Demirci, M. Benekli, M. Oğuz, S. Buyukberber
{"title":"A Case of Extra-Adrenal Paraganglioma Localized in Retroperitoneum Diagnosed With FDG-PET: Case Report and Review of the Literature","authors":"B. Ozturk, U. Coşkun, E. Yaman, O. Akdemir, A. Çakır, L. Memış, K. Sezer, A. Kaya, R. Yıldız, U. Demirci, M. Benekli, M. Oğuz, S. Buyukberber","doi":"10.1097/TEN.0B013E3181D4BF84","DOIUrl":"https://doi.org/10.1097/TEN.0B013E3181D4BF84","url":null,"abstract":"Abstract:Paragangliomas are extremely rare chromaffin cell tumors arising from neural crest cells. Extra-adrenal paragangliomas originate from paravertebral and para-aortic paragangliomas distributed from the skull base to the pelvic floor. Here, we report a 57-year-old woman who presented with abdo","PeriodicalId":50531,"journal":{"name":"Endocrinologist","volume":"15 1","pages":"60-62"},"PeriodicalIF":0.0,"publicationDate":"2010-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82501859","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Milk-Alkali Syndrome—Without Milk 乳碱综合征-无乳
Endocrinologist Pub Date : 2010-03-01 DOI: 10.1097/TEN.0B013E3181D4AAEE
A. Bhansali, Shanmugasundar Gopal, Anantharaman Ramakrishna, P. Ravikumar, S. Bhadada, R. Walia, P. Dutta
{"title":"Milk-Alkali Syndrome—Without Milk","authors":"A. Bhansali, Shanmugasundar Gopal, Anantharaman Ramakrishna, P. Ravikumar, S. Bhadada, R. Walia, P. Dutta","doi":"10.1097/TEN.0B013E3181D4AAEE","DOIUrl":"https://doi.org/10.1097/TEN.0B013E3181D4AAEE","url":null,"abstract":"","PeriodicalId":50531,"journal":{"name":"Endocrinologist","volume":"150 1","pages":"48-49"},"PeriodicalIF":0.0,"publicationDate":"2010-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74853828","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Severe Thyrotoxicosis in a Patient With Extra-Adrenal Pheochromocytoma: Two Disorders With a Similar Clinical Presentation 肾上腺外嗜铬细胞瘤患者的严重甲状腺毒症:两种具有相似临床表现的疾病
Endocrinologist Pub Date : 2010-03-01 DOI: 10.1097/TEN.0B013E3181D4BE5D
B. Laway, S. Rehman, M. Ganie, K. Wani, R. Wani, A. Hakeem, M. I. Lone, A. Zargar
{"title":"Severe Thyrotoxicosis in a Patient With Extra-Adrenal Pheochromocytoma: Two Disorders With a Similar Clinical Presentation","authors":"B. Laway, S. Rehman, M. Ganie, K. Wani, R. Wani, A. Hakeem, M. I. Lone, A. Zargar","doi":"10.1097/TEN.0B013E3181D4BE5D","DOIUrl":"https://doi.org/10.1097/TEN.0B013E3181D4BE5D","url":null,"abstract":"","PeriodicalId":50531,"journal":{"name":"Endocrinologist","volume":"53 1","pages":"55-57"},"PeriodicalIF":0.0,"publicationDate":"2010-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83107373","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Sinister Cause of High Bone Mass 高骨量的险恶原因
Endocrinologist Pub Date : 2010-03-01 DOI: 10.1097/TEN.0B013E3181D2199B
A. Rogstad, B. Meisenberg, E. McCarthy, E. Streeten
{"title":"A Sinister Cause of High Bone Mass","authors":"A. Rogstad, B. Meisenberg, E. McCarthy, E. Streeten","doi":"10.1097/TEN.0B013E3181D2199B","DOIUrl":"https://doi.org/10.1097/TEN.0B013E3181D2199B","url":null,"abstract":"","PeriodicalId":50531,"journal":{"name":"Endocrinologist","volume":"12 1","pages":"80-82"},"PeriodicalIF":0.0,"publicationDate":"2010-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"81043678","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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