A searchable database of
medically documented cases

About the Project

Spontaneous Remission Of Isaacs’ Syndrome

Uslu, S. 2019Adrenal tumor

Uslu, S., Yüce İnel, T., Karakaş, A., & Önen, F. (2019). Spontaneous Remission of Isaacs’ Syndrome. Balkan medical journal, 36(4), 251–252. https://doi.org/10.4274/balkanmedj.galenos.2019.2019.2.53

View Original Source →

Abstract

An 18-year-old man presented with generalized body ache, muscle cramps, weight loss, and painful muscle twitching in his lower extremities.His symptoms aggravated with physical exertion.There was an increased sweating on his limbs and trunk.His medical history was notable for lichen planus.He was a nonsmoker and did not use illicit drugs.Family history was insignificant.On examination, fasciculations on his lower extremities were observed (Video 1).Consciousness, mental state, tone, power, reflexes, senses, cerebellar signs, and cranial nerves on examination were normal.Laboratory investigations of the patient revealed elevated muscle enzymes: creatine phosphokinase as 922 U/L (0-171 U/L), aspartate aminotransferase as 85 U/L (0-50 U/L), and alanine aminotransferase as 157 U/L (0-50 U/L).Serum electrolytes, thyroid hormone, calcium, phosphate, and vitamin D levels were normal.The expression of anti-nuclear, antineutrophil cytoplasmic, and extractable nuclear antibodies was negative.Magnetic resonance imaging showed no evidence of myositis, and the cranial magnetic resonance imaging was normal.A written informed consent was obtained from the patient.Nerve conduction studies revealed normal electrophysiological findings.However, a decremental response to repetitive nerve

Case Details

Disease Location

Muscle

Personal Characteristics

18-year-old man. Smoker. History of lichen planus

Clinical Characteristics

Presented with generalized body aches, muscle cramps, weight loss, and painful muscle twitching in his lower extremities. His symptoms are aggravated with physical exertion. On examination, fasciculations on his lower extremities were observed. Laboratory investigations of the patient revealed elevated muscle enzymes: creatine phosphokinase, aspartate aminotransferase, and alanine aminotransferase. Needle electromyography examination revealed spontaneous motor unit potential transitions and fasciculations in the gastrocnemius muscle. The concentration of serum anti-voltage-gated potassium channel antibodies was elevated. A diagnosis of isaacs’ syndrome was made

Remission Characteristics

While further investigations were in progress, the patient recovered spontaneously without treatment.

Treatment & Mechanisms