|
Neurology India, Vol. 57, No. 4, July-August, 2009, pp. 501 Letter To Editor A case of sporadic periodic hypokalemic paralysis with atypical features: Recurrent differential right brachial weakness and cognitive dysfunction A. N. Joshi, A. P. Jain, A. D. Bhatt, S. Kumar Department of Medicine, Mahatma Gandhi Institute of Medical Sciences, Sewagram, Wardha, Maharashtra, India Correspondence Address: Department of Medicine, Mahatma Gandhi Institute of Medical Sciences, Sewagram, Wardha, Maharashtra, India, dr.anjalijoshi@gmail.com Date of Acceptance: 25-Feb-2009 Code Number: ni09141 PMID: 19770562 DOI: 10.4103/0028-3886.55581 Sir, We present a case of 28-year-old man admitted with an episode of fall due to weakness in all four limbs, with differential weakness of right upper limb that was associated with cognitive dysfunction. He had experienced multiple episodes of such attacks in the past 10 years. The relatives also noticed that after such an attack the patient remained confused for few hours. He did not give history of palpitations, hand tremors, or heat intolerance. His computed tomography scan of head and electroencephalogram suggested no abnormality. MRI of the brain was not done. A short review of systems was otherwise noncontributory. Neurological examination revealed the overall power in limbs was about 4/5, but in the right upper limb it was found to be 1/5. There was generalized hyporeflexia with a flexor plantars. His score on mini mental state examination (MMSE) was 21/30. The remainder of the physical examinations was noncontributory. Serum electrolyte: Potassium 1.7mEq/L (normal range: 3.5-5.3mEq/L). He was investigated for renal loss of potassium which was normal. His thyroid stimulating hormone level (TSH) was reduced to 0.05ng/dL (normal range: 0.45-4.5ng/dL) indicating a hyperthyroid state. He was given potassium supplementation after which his symptoms recovered completely along with improvement of cognitive functions without any residual weakness. His nerve conduction velocity (NCV) done during a nonparalyzed state was normal. Periodic hypokalemic paralysis is often unrecognized when first encountered because of its relative rarity.[1] Atypical presentations of severe hypokalemia may be in the form of total paralysis including respiratory, bulbar, and cranial musculature. [2] Some patients complain of muscular weakness, especially of the lower extremities, while marked and generalized weakness of skeletal muscles is common with more severe potassium depletion, but they may present as weakness of specific group of muscles. Sudden deaths from respiratory failure and arrhythmia like ventricular tachycardia and fibrillation have been reported.[3],[4],[5] Our case was typical in presence of marked generalized weakness with differential weakness of right upper limb, reason of which cannot be explained. The sensations and level of consciousness are generally unaffected. Our patient had history of cognitive disturbance during the attack with hyporeflexia in all four limbs. Cognitive disturbances with hypokalemia have not been reported in literature. Both of the problems improved completely after potassium replacement which is a prerequisite for diagnosis of this disease. References
Copyright 2009 - Neurology India |
|