Thyrotoxic Vomiting: A Case Report and Possible Mechanisms

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چکیده

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Thyrotoxic Vomiting: A Case Report and Possible Mechanisms

The symptoms related to gastrointestinal (GI) tract are sometimes chief complaints in patients with endocrine disease. Thyrotoxicosis is a rare, but notable cause for unexplained and repeated vomiting. Here, we report an adolescent patient with thyrotoxicosis who was initially presented with repeated vomiting and epigastric pain. A 13-year-old female was referred to a GI outpatient department f...

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Thyrotoxic periodic paralysis: A case report

A 28-year-old Filipino gentleman mechanical engineer without any medical problem admitted to our hospital on 16th of February 2016 with complains of numbness and weakness in lower limbs when he woke up for urination at around 3:00 am on the day of admission which started distally symmetrically and progressed proximally and gradually involved the upper limbs in the same pattern, the proximal mus...

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[Thyrotoxic hypokalemic periodic paralysis. A case report].

Thyrotoxic hypokalemic periodic paralysis is an uncommon complication of thyrotoxicosis, characterized by attacks of generalized muscular weakness associated with hypokalemia in patients with hyperthyroidism, most frequently with Graves-Basedow disease. Treatment with antithyroid drugs and potassium supplements reversed the symptoms and the episodes of acute muscular weakness did not reappear.

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Thyrotoxic hypokalemic paralysis: a case report

Transient periodical muscle paralysis is an important neurological presentation. Thyrotoxic hypokalemic paralysis is an uncommon type of thyrotoxic paralysis. Except for the findings specifically caused by the subtle hyperthyroid state the clinical and biochemical features of thyrotoxic hypokalemic paralysis are identical to those of familial periodic paralysis. In this article, a case of a 26 ...

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Thyrotoxic periodic paralysis-A case report.

Thyrotoxic periodic paralysis (TPP) is characterized by recurrent episodes of muscle weakness and hypokalemia associated with thyroid hyperactivity. Reported predominantly among individuals of Asian descent, TPP is a rare manifestation of hyperthyroidism in western populations. We describe a typical case of TPP in a 33-year-old portuguese male, who presented with acute tetraparesis associated w...

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ژورنال

عنوان ژورنال: Journal of Neurogastroenterology and Motility

سال: 2010

ISSN: 2093-0879,2093-0887

DOI: 10.5056/jnm.2010.16.4.428