Pub Date : 2010-03-01DOI: 10.1097/TEN.0B013E3181D4BF70
J. George, V. Sarathi, T. Bandgar, P. Menon, N. Shah
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.
{"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}
Pub Date : 2010-03-01DOI: 10.1097/TEN.0B013E3181D4AB73
Xiu-jing Wu, Li-hua Chen, Ya-ping Xu
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.
{"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}
Pub Date : 2010-03-01DOI: 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}
Pub Date : 2010-03-01DOI: 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}
Pub Date : 2010-03-01DOI: 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}
Pub Date : 2010-03-01DOI: 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}
Pub Date : 2010-03-01DOI: 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
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
{"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}
Pub Date : 2010-03-01DOI: 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}
Pub Date : 2010-03-01DOI: 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}
Pub Date : 2010-03-01DOI: 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}
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