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Severe Thyrotoxicosis Secondary to Povidone-Iodine from Peritoneal Dialysis.

Case reports in endocrinology

Lithgow K, Symonds C.
PMID: 28912982
Case Rep Endocrinol. 2017;2017:2683120. doi: 10.1155/2017/2683120. Epub 2017 Aug 24.

A 73-year-old male on home peritoneal dialysis (PD) with recent diagnosis of atrial fibrillation presented with fatigue and dyspnea. Hyperthyroidism was diagnosed with TSH < 0.01 mIU/L and FT4 > 100 pmol/L. He had no personal or family history...

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Lithgow K, Symonds C. Severe Thyrotoxicosis Secondary to Povidone-Iodine from Peritoneal Dialysis. Case Rep Endocrinol. 2017;2017:2683120doi: 10.1155/2017/2683120.
Lithgow, K., & Symonds, C. (2017). Severe Thyrotoxicosis Secondary to Povidone-Iodine from Peritoneal Dialysis. Case reports in endocrinology, 20172683120. https://doi.org/10.1155/2017/2683120
Lithgow, Kirstie, and Symonds, Christopher. "Severe Thyrotoxicosis Secondary to Povidone-Iodine from Peritoneal Dialysis." Case reports in endocrinology vol. 2017 (2017): 2683120. doi: https://doi.org/10.1155/2017/2683120
Lithgow K, Symonds C. Severe Thyrotoxicosis Secondary to Povidone-Iodine from Peritoneal Dialysis. Case Rep Endocrinol. 2017;2017:2683120. doi: 10.1155/2017/2683120. Epub 2017 Aug 24. PMID: 28912982; PMCID: PMC5587962.
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Anaplastic Spindle Cell Squamous Carcinoma Arising from Tall Cell Variant Papillary Carcinoma of the Thyroid Gland: A Case Report and Review of the Literature.

Case reports in endocrinology

Patten DK, Ahmed A, Greaves O, Dina R, Flora R, Tolley N.
PMID: 28484653
Case Rep Endocrinol. 2017;2017:4581626. doi: 10.1155/2017/4581626. Epub 2017 Apr 06.

Tall cell variant (TCV) of papillary thyroid carcinoma (PTC), an aggressive form of thyroid cancer, is characterised by 50% of cells with height that is three times greater than the width. Very rarely, some of these cancers can progress...

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Patten DK, Ahmed A, Greaves O, et al. Anaplastic Spindle Cell Squamous Carcinoma Arising from Tall Cell Variant Papillary Carcinoma of the Thyroid Gland: A Case Report and Review of the Literature. Case Rep Endocrinol. 2017;2017:4581626doi: 10.1155/2017/4581626.
Patten, D. K., Ahmed, A., Greaves, O., Dina, R., Flora, R., & Tolley, N. (2017). Anaplastic Spindle Cell Squamous Carcinoma Arising from Tall Cell Variant Papillary Carcinoma of the Thyroid Gland: A Case Report and Review of the Literature. Case reports in endocrinology, 20174581626. https://doi.org/10.1155/2017/4581626
Patten, Darren K, et al. "Anaplastic Spindle Cell Squamous Carcinoma Arising from Tall Cell Variant Papillary Carcinoma of the Thyroid Gland: A Case Report and Review of the Literature." Case reports in endocrinology vol. 2017 (2017): 4581626. doi: https://doi.org/10.1155/2017/4581626
Patten DK, Ahmed A, Greaves O, Dina R, Flora R, Tolley N. Anaplastic Spindle Cell Squamous Carcinoma Arising from Tall Cell Variant Papillary Carcinoma of the Thyroid Gland: A Case Report and Review of the Literature. Case Rep Endocrinol. 2017;2017:4581626. doi: 10.1155/2017/4581626. Epub 2017 Apr 06. PMID: 28484653; PMCID: PMC5397626.
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Short Stature Homeobox-Containing Haploinsufficiency in Seven Siblings with Short Stature.

Case reports in endocrinology

Sandberg ES, Calikoglu AS, Loechner KJ, Snyder LL.
PMID: 28948052
Case Rep Endocrinol. 2017;2017:7287351. doi: 10.1155/2017/7287351. Epub 2017 Aug 30.

Deficiency of the short stature homeobox-containing (SHOX) gene is a frequent cause of short stature in children (2-15%). Here, we report 7 siblings with SHOX deficiency due to a point mutation in the SHOX gene. Index case was a...

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Sandberg ES, Calikoglu AS, Loechner KJ, et al. Short Stature Homeobox-Containing Haploinsufficiency in Seven Siblings with Short Stature. Case Rep Endocrinol. 2017;2017:7287351doi: 10.1155/2017/7287351.
Sandberg, E. S., Calikoglu, A. S., Loechner, K. J., & Snyder, L. L. (2017). Short Stature Homeobox-Containing Haploinsufficiency in Seven Siblings with Short Stature. Case reports in endocrinology, 20177287351. https://doi.org/10.1155/2017/7287351
Sandberg, Elizabeth S, et al. "Short Stature Homeobox-Containing Haploinsufficiency in Seven Siblings with Short Stature." Case reports in endocrinology vol. 2017 (2017): 7287351. doi: https://doi.org/10.1155/2017/7287351
Sandberg ES, Calikoglu AS, Loechner KJ, Snyder LL. Short Stature Homeobox-Containing Haploinsufficiency in Seven Siblings with Short Stature. Case Rep Endocrinol. 2017;2017:7287351. doi: 10.1155/2017/7287351. Epub 2017 Aug 30. PMID: 28948052; PMCID: PMC5602651.
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Development of Agranulocytosis after Discontinuation of Methimazole: An Unusual Case.

Case reports in endocrinology

Üçler R, Atmaca M, Candar Ö, Alay M, Göy B, Kara E, Turan M, Demir Y.
PMID: 26339512
Case Rep Endocrinol. 2015;2015:974524. doi: 10.1155/2015/974524. Epub 2015 Aug 03.

Agranulocytosis is a rare and critical adverse effect of antithyroid drugs (ATD). The occurrence of agranulocytosis in continuous ATD treatment patients is well known; however, a case of ATD agranulocytosis occurring following the discontinuation of methimazole (MMI) treatment is...

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Üçler R, Atmaca M, Candar Ö, et al. Development of Agranulocytosis after Discontinuation of Methimazole: An Unusual Case. Case Rep Endocrinol. 2015;2015:974524doi: 10.1155/2015/974524.
Üçler, R., Atmaca, M., Candar, �. �., Alay, M., Göy, B., Kara, E., Turan, M., & Demir, Y. (2015). Development of Agranulocytosis after Discontinuation of Methimazole: An Unusual Case. Case reports in endocrinology, 2015974524. https://doi.org/10.1155/2015/974524
Üçler, Rıfkı, et al. "Development of Agranulocytosis after Discontinuation of Methimazole: An Unusual Case." Case reports in endocrinology vol. 2015 (2015): 974524. doi: https://doi.org/10.1155/2015/974524
Üçler R, Atmaca M, Candar Ö, Alay M, Göy B, Kara E, Turan M, Demir Y. Development of Agranulocytosis after Discontinuation of Methimazole: An Unusual Case. Case Rep Endocrinol. 2015;2015:974524. doi: 10.1155/2015/974524. Epub 2015 Aug 03. PMID: 26339512; PMCID: PMC4538967.
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Congenital Bands with Intestinal Malrotation after Propylthiouracil Exposure in Early Pregnancy.

Case reports in endocrinology

Leung AA, Yamamoto J, Luca P, Beaudry P, McKeen J.
PMID: 26664769
Case Rep Endocrinol. 2015;2015:789762. doi: 10.1155/2015/789762. Epub 2015 Nov 18.

Exposure to propylthiouracil in early pregnancy may be associated with an increased risk of birth defects. But the spectrum of associated congenital anomalies is not yet well defined. While preliminary reports suggest that most cases of propylthiouracil-associated birth defects...

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Leung AA, Yamamoto J, Luca P, et al. Congenital Bands with Intestinal Malrotation after Propylthiouracil Exposure in Early Pregnancy. Case Rep Endocrinol. 2015;2015:789762doi: 10.1155/2015/789762.
Leung, A. A., Yamamoto, J., Luca, P., Beaudry, P., & McKeen, J. (2015). Congenital Bands with Intestinal Malrotation after Propylthiouracil Exposure in Early Pregnancy. Case reports in endocrinology, 2015789762. https://doi.org/10.1155/2015/789762
Leung, Alexander A, et al. "Congenital Bands with Intestinal Malrotation after Propylthiouracil Exposure in Early Pregnancy." Case reports in endocrinology vol. 2015 (2015): 789762. doi: https://doi.org/10.1155/2015/789762
Leung AA, Yamamoto J, Luca P, Beaudry P, McKeen J. Congenital Bands with Intestinal Malrotation after Propylthiouracil Exposure in Early Pregnancy. Case Rep Endocrinol. 2015;2015:789762. doi: 10.1155/2015/789762. Epub 2015 Nov 18. PMID: 26664769; PMCID: PMC4667016.
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Characteristics and Treatment Results of 5 Patients with Fibrous Dysplasia and Review of the Literature.

Case reports in endocrinology

Ozdemir Kutbay N, Sarer Yurekli B, Kartal Baykan E, Baydur Sahin S, Saygili F.
PMID: 26171261
Case Rep Endocrinol. 2015;2015:670809. doi: 10.1155/2015/670809. Epub 2015 Jun 14.

Aim. Fibrous dysplasia is a rare bone disease caused by missense mutation leading to abnormal fibroblast and osteoblast proliferation and increased bone resorption. FD can present in monostotic or polyostotic forms. About 3% of FD could be in association...

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Ozdemir Kutbay N, Sarer Yurekli B, Kartal Baykan E, et al. Characteristics and Treatment Results of 5 Patients with Fibrous Dysplasia and Review of the Literature. Case Rep Endocrinol. 2015;2015:670809doi: 10.1155/2015/670809.
Ozdemir Kutbay, N., Sarer Yurekli, B., Kartal Baykan, E., Baydur Sahin, S., & Saygili, F. (2015). Characteristics and Treatment Results of 5 Patients with Fibrous Dysplasia and Review of the Literature. Case reports in endocrinology, 2015670809. https://doi.org/10.1155/2015/670809
Ozdemir Kutbay, Nilufer, et al. "Characteristics and Treatment Results of 5 Patients with Fibrous Dysplasia and Review of the Literature." Case reports in endocrinology vol. 2015 (2015): 670809. doi: https://doi.org/10.1155/2015/670809
Ozdemir Kutbay N, Sarer Yurekli B, Kartal Baykan E, Baydur Sahin S, Saygili F. Characteristics and Treatment Results of 5 Patients with Fibrous Dysplasia and Review of the Literature. Case Rep Endocrinol. 2015;2015:670809. doi: 10.1155/2015/670809. Epub 2015 Jun 14. PMID: 26171261; PMCID: PMC4480246.
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A 33-Year-Old Man with Gynaecomastia and Galactorrhea as the First Symptoms of Graves Hyperthyroidism.

Case reports in endocrinology

Khoohaphatthanakul S, Sriwijitkamol A.
PMID: 28044109
Case Rep Endocrinol. 2016;2016:1946824. doi: 10.1155/2016/1946824. Epub 2016 Dec 01.

Graves' hyperthyroidism has a various number of well-recognized manifestations. Galactorrhea is a rare manifestation in this disease. We describe a 33-year-old man who presented with the symptoms of hyperthyroidism, gynaecomastia, and galactorrhea for 2 months. Physical examination revealed goitre,...

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Khoohaphatthanakul S, Sriwijitkamol A. A 33-Year-Old Man with Gynaecomastia and Galactorrhea as the First Symptoms of Graves Hyperthyroidism. Case Rep Endocrinol. 2016;2016:1946824doi: 10.1155/2016/1946824.
Khoohaphatthanakul, S., & Sriwijitkamol, A. (2016). A 33-Year-Old Man with Gynaecomastia and Galactorrhea as the First Symptoms of Graves Hyperthyroidism. Case reports in endocrinology, 20161946824. https://doi.org/10.1155/2016/1946824
Khoohaphatthanakul, Somdul, and Sriwijitkamol, Apiradee. "A 33-Year-Old Man with Gynaecomastia and Galactorrhea as the First Symptoms of Graves Hyperthyroidism." Case reports in endocrinology vol. 2016 (2016): 1946824. doi: https://doi.org/10.1155/2016/1946824
Khoohaphatthanakul S, Sriwijitkamol A. A 33-Year-Old Man with Gynaecomastia and Galactorrhea as the First Symptoms of Graves Hyperthyroidism. Case Rep Endocrinol. 2016;2016:1946824. doi: 10.1155/2016/1946824. Epub 2016 Dec 01. PMID: 28044109; PMCID: PMC5156789.
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The Biochemical Profile of Familial Hypocalciuric Hypercalcemia and Primary Hyperparathyroidism during Pregnancy and Lactation: Two Case Reports and Review of the Literature.

Case reports in endocrinology

Ghaznavi SA, Saad NM, Donovan LE.
PMID: 27957351
Case Rep Endocrinol. 2016;2016:2725486. doi: 10.1155/2016/2725486. Epub 2016 Nov 09.

No abstract available.

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Ghaznavi SA, Saad NM, Donovan LE. The Biochemical Profile of Familial Hypocalciuric Hypercalcemia and Primary Hyperparathyroidism during Pregnancy and Lactation: Two Case Reports and Review of the Literature. Case Rep Endocrinol. 2016;2016:2725486doi: 10.1155/2016/2725486.
Ghaznavi, S. A., Saad, N. M., & Donovan, L. E. (2016). The Biochemical Profile of Familial Hypocalciuric Hypercalcemia and Primary Hyperparathyroidism during Pregnancy and Lactation: Two Case Reports and Review of the Literature. Case reports in endocrinology, 20162725486. https://doi.org/10.1155/2016/2725486
Ghaznavi, S A, et al. "The Biochemical Profile of Familial Hypocalciuric Hypercalcemia and Primary Hyperparathyroidism during Pregnancy and Lactation: Two Case Reports and Review of the Literature." Case reports in endocrinology vol. 2016 (2016): 2725486. doi: https://doi.org/10.1155/2016/2725486
Ghaznavi SA, Saad NM, Donovan LE. The Biochemical Profile of Familial Hypocalciuric Hypercalcemia and Primary Hyperparathyroidism during Pregnancy and Lactation: Two Case Reports and Review of the Literature. Case Rep Endocrinol. 2016;2016:2725486. doi: 10.1155/2016/2725486. Epub 2016 Nov 09. PMID: 27957351; PMCID: PMC5120212.
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Nonislet Cell Tumor Hypoglycemia in a Patient with Adrenal Cortical Carcinoma.

Case reports in endocrinology

Kim SW, Lee SE, Oh YL, Kim S, Park SH, Kim JH.
PMID: 27957352
Case Rep Endocrinol. 2016;2016:5731417. doi: 10.1155/2016/5731417. Epub 2016 Nov 10.

Nonislet cell tumor hypoglycemia (NICTH) is a rare but serious paraneoplastic syndrome in which a tumor secretes incompletely processed precursors of insulin-like growth factor-II (IGF-II), causing hypoglycemia. Here, we report an exceptional case of NICTH caused by nonfunctioning adrenocortical...

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Kim SW, Lee SE, Oh YL, et al. Nonislet Cell Tumor Hypoglycemia in a Patient with Adrenal Cortical Carcinoma. Case Rep Endocrinol. 2016;2016:5731417doi: 10.1155/2016/5731417.
Kim, S. W., Lee, S. E., Oh, Y. L., Kim, S., Park, S. H., & Kim, J. H. (2016). Nonislet Cell Tumor Hypoglycemia in a Patient with Adrenal Cortical Carcinoma. Case reports in endocrinology, 20165731417. https://doi.org/10.1155/2016/5731417
Kim, Se Won, et al. "Nonislet Cell Tumor Hypoglycemia in a Patient with Adrenal Cortical Carcinoma." Case reports in endocrinology vol. 2016 (2016): 5731417. doi: https://doi.org/10.1155/2016/5731417
Kim SW, Lee SE, Oh YL, Kim S, Park SH, Kim JH. Nonislet Cell Tumor Hypoglycemia in a Patient with Adrenal Cortical Carcinoma. Case Rep Endocrinol. 2016;2016:5731417. doi: 10.1155/2016/5731417. Epub 2016 Nov 10. PMID: 27957352; PMCID: PMC5121447.
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Occult Langerhans Cell Histiocytosis Presenting with Papillary Thyroid Carcinoma, a Thickened Pituitary Stalk and Diabetes Insipidus.

Case reports in endocrinology

Gordon MS, Gordon MB.
PMID: 27656301
Case Rep Endocrinol. 2016;2016:5191903. doi: 10.1155/2016/5191903. Epub 2016 Aug 30.

Etiologies of a thickened stalk include inflammatory, neoplastic, and idiopathic origins, and the underlying diagnosis may remain occult. We report a patient with a thickened pituitary stalk (TPS) and papillary thyroid carcinoma (PTC) whose diagnosis remained obscure until a...

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Gordon MS, Gordon MB. Occult Langerhans Cell Histiocytosis Presenting with Papillary Thyroid Carcinoma, a Thickened Pituitary Stalk and Diabetes Insipidus. Case Rep Endocrinol. 2016;2016:5191903doi: 10.1155/2016/5191903.
Gordon, M. S., & Gordon, M. B. (2016). Occult Langerhans Cell Histiocytosis Presenting with Papillary Thyroid Carcinoma, a Thickened Pituitary Stalk and Diabetes Insipidus. Case reports in endocrinology, 20165191903. https://doi.org/10.1155/2016/5191903
Gordon, Michael S, and Gordon, Murray B. "Occult Langerhans Cell Histiocytosis Presenting with Papillary Thyroid Carcinoma, a Thickened Pituitary Stalk and Diabetes Insipidus." Case reports in endocrinology vol. 2016 (2016): 5191903. doi: https://doi.org/10.1155/2016/5191903
Gordon MS, Gordon MB. Occult Langerhans Cell Histiocytosis Presenting with Papillary Thyroid Carcinoma, a Thickened Pituitary Stalk and Diabetes Insipidus. Case Rep Endocrinol. 2016;2016:5191903. doi: 10.1155/2016/5191903. Epub 2016 Aug 30. PMID: 27656301; PMCID: PMC5021458.
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Amyloid Goiter Secondary to Ulcerative Colitis.

Case reports in endocrinology

Aydin B, Koca YS, Koca T, Yildiz I, Gerek Celikden S, Ciris M.
PMID: 27051538
Case Rep Endocrinol. 2016;2016:3240585. doi: 10.1155/2016/3240585. Epub 2016 Mar 08.

Diffuse amyloid goiter (AG) is an entity characterized by the deposition of amyloid in the thyroid gland. AG may be associated with either primary or secondary amyloidosis. Secondary amyloidosis is rarely caused by inflammatory bowel diseases. Secondary amyloidosis is...

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Aydin B, Koca YS, Koca T, et al. Amyloid Goiter Secondary to Ulcerative Colitis. Case Rep Endocrinol. 2016;2016:3240585doi: 10.1155/2016/3240585.
Aydin, B., Koca, Y. S., Koca, T., Yildiz, I., Gerek Celikden, S., & Ciris, M. (2016). Amyloid Goiter Secondary to Ulcerative Colitis. Case reports in endocrinology, 20163240585. https://doi.org/10.1155/2016/3240585
Aydin, Bunyamin, et al. "Amyloid Goiter Secondary to Ulcerative Colitis." Case reports in endocrinology vol. 2016 (2016): 3240585. doi: https://doi.org/10.1155/2016/3240585
Aydin B, Koca YS, Koca T, Yildiz I, Gerek Celikden S, Ciris M. Amyloid Goiter Secondary to Ulcerative Colitis. Case Rep Endocrinol. 2016;2016:3240585. doi: 10.1155/2016/3240585. Epub 2016 Mar 08. PMID: 27051538; PMCID: PMC4802030.
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Hypochondroplasia, Acanthosis Nigricans, and Insulin Resistance in a Child with FGFR3 Mutation: Is It Just an Association?.

Case reports in endocrinology

Mustafa M, Moghrabi N, Bin-Abbas B.
PMID: 25505998
Case Rep Endocrinol. 2014;2014:840492. doi: 10.1155/2014/840492. Epub 2014 Nov 19.

FGFR3 mutations cause wide spectrum of disorders ranging from skeletal dysplasias (hypochondroplasia, achondroplasia, and thanatophoric dysplasia), benign skin tumors (epidermal nevi, seborrhaeic keratosis, and acanthosis nigricans), and epithelial malignancies (multiple myeloma and prostate and bladder carcinoma). Hypochondroplasia is the...

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Mustafa M, Moghrabi N, Bin-Abbas B. Hypochondroplasia, Acanthosis Nigricans, and Insulin Resistance in a Child with FGFR3 Mutation: Is It Just an Association?. Case Rep Endocrinol. 2014;2014:840492doi: 10.1155/2014/840492.
Mustafa, M., Moghrabi, N., & Bin-Abbas, B. (2014). Hypochondroplasia, Acanthosis Nigricans, and Insulin Resistance in a Child with FGFR3 Mutation: Is It Just an Association?. Case reports in endocrinology, 2014840492. https://doi.org/10.1155/2014/840492
Mustafa, Manal, et al. "Hypochondroplasia, Acanthosis Nigricans, and Insulin Resistance in a Child with FGFR3 Mutation: Is It Just an Association?." Case reports in endocrinology vol. 2014 (2014): 840492. doi: https://doi.org/10.1155/2014/840492
Mustafa M, Moghrabi N, Bin-Abbas B. Hypochondroplasia, Acanthosis Nigricans, and Insulin Resistance in a Child with FGFR3 Mutation: Is It Just an Association?. Case Rep Endocrinol. 2014;2014:840492. doi: 10.1155/2014/840492. Epub 2014 Nov 19. PMID: 25505998; PMCID: PMC4255054.
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Showing 1 to 12 of 578 entries