Cargando…

Gynecomastia as a presenting symptom of Graves’ disease in a 49-year-old man

SUMMARY: Gynecomastia is a symptom with a potential high disease burden. It has a variety of underlying causes, such as malignant, drug-related or hormonal. The presence of gynecomastia can be explained in thyrotoxicosis due to a concomitant disbalance of sex hormones. Interestingly, it rarely is th...

Descripción completa

Detalles Bibliográficos
Autores principales:	Mohammadnia, N, Simsek, S, Stam, F
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Bioscientifica Ltd 2021
Materias:	Insight into Disease Pathogenesis or Mechanism of Therapy
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8115411/ https://www.ncbi.nlm.nih.gov/pubmed/33880994 http://dx.doi.org/10.1530/EDM-20-0181

Ejemplares similares

Asymptomatic Paget's disease of bone in a 62-year-old Nigerian man: three years post-alendronate therapy
por: Aransiola, Clement Olukayode, et al.
Publicado: (2016)

Managing thymic enlargement in Graves’ disease
por: Kamath, C, et al.
Publicado: (2019)

Thyroid antibody-negative euthyroid Graves’ ophthalmopathy
por: Tabasum, Arshiya, et al.
Publicado: (2016)

Thyrotoxic periodic paralysis associated with Graves’ disease: a case series
por: Ludgate, S, et al.
Publicado: (2022)

Antithyroid arthritis syndrome caused by methimazole in a patient with Graves’ disease
por: Kawasumi, Muneo, et al.
Publicado: (2023)

Propylthiouracil-induced antineutrophil cytoplasmic antibody-associated vasculitis and agranulocytosis in a patient with Graves’ disease
por: Tomkins, Maria, et al.
Publicado: (2019)

Anterior hypopituitarism secondary to biopsy-proven IgG4-related hypophysitis in a young man
por: Joshi, H, et al.
Publicado: (2019)

Continuous glucose monitoring in a patient with insulinoma presenting with unawareness of postprandial hypoglycemia
por: Nakajima, Rikako, et al.
Publicado: (2023)

Diabetes mellitus-induced lower urinary tract symptoms and hepatic steatosis in an older male
por: Opara, Nnennaya U
Publicado: (2022)

Rare distant metastases to pancreas, liver, and lung as initial presentation of mixed tall cell and columnar cell variants of papillary thyroid cancer
por: Harper, Cody, et al.
Publicado: (2022)

The possibilities and impossibilities of treating acromegaly 50 years ago illustrated by the Diane Arbus photograph, A Jewish giant at home with his parents in the Bronx, N.Y. 1970
por: de Herder, Wouter W.
Publicado: (2021)

A clinically novel AIP mutation in a patient with a very large, apparently sporadic somatotrope adenoma
por: Salvatori, Roberto, et al.
Publicado: (2014)

Identification of a TMEM127 variant in a patient with paraganglioma and acromegaly
por: Stütz, Beryl, et al.
Publicado: (2020)

Milk-alkali syndrome: a ‘quick ease’ or a ‘long-lasting problem’
por: Wang, Mawson, et al.
Publicado: (2020)

Starvation ketosis in a pregnant woman with COVID-19: a case report
por: Nana, Melanie, et al.
Publicado: (2022)

Identification of a novel large CASR deletion in a patient with familial hypocalciuric hypercalcemia
por: García-Castaño, Alejandro, et al.
Publicado: (2018)

Impact of a novel 14 bp MEN1 deletion in a patient with hyperparathyroidism and gastrinoma
por: Birla, Shweta, et al.
Publicado: (2015)

Growth of a progesterone receptor-positive meningioma in a female patient with congenital adrenal hyperplasia
por: O’Shea, T, et al.
Publicado: (2016)

Rapid response to leptin therapy in a FPLD patient with a novel PPARG missense variant
por: Melzer, Fiona, et al.
Publicado: (2021)

Testosterone-induced increase in libido in a patient with a loss-of-function mutation in the AR gene
por: Marino, Laura, et al.
Publicado: (2021)

Identification of a novel hepatocyte nuclear factor-1 alpha (HNF1A) variant in maturity onset diabetes of the young type 3 (HNF1A-MODY)
por: Verma, Megha, et al.
Publicado: (2022)

Perioperative control of paroxysmal hypertension using esmolol with alpha-blockade in a child with a germline mutated paraganglioma
por: Babiker, Amir, et al.
Publicado: (2021)

Acromegaly caused by a GHRH-producing pancreatic neuroendocrine tumor: a rare manifestation of MEN1 syndrome
por: Koivikko, Minna, et al.
Publicado: (2022)

First reported case in Ireland of MEN2A due to a rare mutation in exon 8 of the RET oncogene
por: Casey, R, et al.
Publicado: (2013)

Identification of a novel heterozygous mutation in exon 50 of the COL1A1 gene causing osteogenesis imperfecta
por: Aftab, S A S, et al.
Publicado: (2013)

A rare cause of primary adrenal insufficiency due to a homozygous Arg188Cys mutation in the STAR gene
por: Burget, Lukas, et al.
Publicado: (2018)

Silent gonadotroph pituitary neuroendocrine tumor in a patient with tuberous sclerosis complex: evaluation of a possible molecular link
por: Regazzo, Daniela, et al.
Publicado: (2018)

Recurrent vertebral fractures in a young adult: a closer look at bone health in type 1 diabetes mellitus
por: Thong, Eleanor P, et al.
Publicado: (2018)

A case of NASH with genetic predisposition successfully treated with an SGLT2 inhibitor: a possible involvement of mitochondrial dysfunction
por: Nakajima, Rikako, et al.
Publicado: (2022)

A rare cause of severe Cushing’s syndrome
por: Zaman, Shamaila, et al.
Publicado: (2020)

A case of early-onset diabetes with impaired insulin secretion carrying a PAX6 gene Gln135* mutation
por: Sekiya, Motohiro, et al.
Publicado: (2022)

Pheochromocytomatosis associated with a novel TMEM127 mutation
por: Yu, Run, et al.
Publicado: (2017)

A novel splice-site mutation of the HNF1B gene in a family with maturity onset diabetes of the young type 5 (MODY5)
por: Fujita, Yuki, et al.
Publicado: (2020)

Xanthogranulomatous hypophysitis: a rare and often mistaken pituitary lesion
por: Gopal-Kothandapani, Jaya Sujatha, et al.
Publicado: (2015)

Insulin Autoimmune Syndrome: a rare cause of postprandial hypoglycemia
por: Sahni, Pooja, et al.
Publicado: (2016)

Refractory hypoglycemia in a patient with functional adrenal cortical carcinoma
por: Marchetti, Katia Regina, et al.
Publicado: (2016)

Livedo reticularis: a cutaneous clue to an underlying endocrine crisis
por: Shrikrishnapalasuriyar, Natasha, et al.
Publicado: (2018)

ACTH-secreting medullary thyroid cancer: a case series
por: Wijewardene, Ayanthi A, et al.
Publicado: (2017)

Induction of lactation in a patient with complete androgen insensitivity syndrome
por: Voon, Kimberly, et al.
Publicado: (2023)

Autoimmune alternating hyper- and hypo-thyroidism: a rare condition in pediatrics
por: Martins, Luísa Correia, et al.
Publicado: (2016)

Cannot write session to /tmp/vufind_sessions/sess_pq52gc1kv345fogu1djs57dtqg