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AN INTRESTING CASE OF RHABDOMYOLYSIS SECONDARY TO CEREBRAL SYPHILITIC GUMMA IN YOUNG ADULT
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Rhabdomyolysis, a potentially life-threatening condition characterized by the breakdown of skeletal muscle tissue and
release of intracellular contents, commonly occurs in response to trauma, prolonged immobilization, and certain
medications(1). However, its occurrence secondary to neurological disorders, such as cerebral syphilitic gumma, is
exceedingly rare(3). Cerebral syphilitic gumma, a tertiary manifestation of syphilis, presents as granulomatous lesions
in the brain, typically causing neurological symptoms. The co-occurrence of rhabdomyolysis with syphilitic gumma,
though unusual, may reflect the multifactorial impact of neuromuscular compromise such as seizures, prolonged
immobilization, and metabolic disturbances triggered by central nervous system pathology(8). We report a case of a 24-
year-old male who presented with complaints of involuntary movements of bilateral upper and lower limbs, headache,
and difficulty in walking. Laboratory findings revealed elevated creatinine kinase levels (1239 mcg/L), myoglobinuria
(>3000 ng/mL) and creatinine 4.2mg/dl leading to initial diagnosis of rhabdomyolysis. MRI of the brain showed a welldefined, ring-enhancing lesion in the right frontal lobe. VDRL serology was reactive and treponema antibody positive.
Diagnosis was revised to rhabdomyolysis with acute kidney injury secondary to cerebral syphilitic gumma. Patient was
stabilised in ED and treated with benzathine penicillin. Patients with tertiary syphilis poses risk for neurological
complications like, focal neurological deficits and convulsions rhabdomyolysis. The incidence of tertiary syphilis has
declined in developed countries, but untreated cases still pose a risk for such rare manifestations. Early recognition and
appropriate management in ED are crucial to prevent severe systemic complications in these patients.
Title: AN INTRESTING CASE OF RHABDOMYOLYSIS SECONDARY TO CEREBRAL SYPHILITIC GUMMA IN YOUNG ADULT
Description:
Rhabdomyolysis, a potentially life-threatening condition characterized by the breakdown of skeletal muscle tissue and
release of intracellular contents, commonly occurs in response to trauma, prolonged immobilization, and certain
medications(1).
However, its occurrence secondary to neurological disorders, such as cerebral syphilitic gumma, is
exceedingly rare(3).
Cerebral syphilitic gumma, a tertiary manifestation of syphilis, presents as granulomatous lesions
in the brain, typically causing neurological symptoms.
The co-occurrence of rhabdomyolysis with syphilitic gumma,
though unusual, may reflect the multifactorial impact of neuromuscular compromise such as seizures, prolonged
immobilization, and metabolic disturbances triggered by central nervous system pathology(8).
We report a case of a 24-
year-old male who presented with complaints of involuntary movements of bilateral upper and lower limbs, headache,
and difficulty in walking.
Laboratory findings revealed elevated creatinine kinase levels (1239 mcg/L), myoglobinuria
(>3000 ng/mL) and creatinine 4.
2mg/dl leading to initial diagnosis of rhabdomyolysis.
MRI of the brain showed a welldefined, ring-enhancing lesion in the right frontal lobe.
VDRL serology was reactive and treponema antibody positive.
Diagnosis was revised to rhabdomyolysis with acute kidney injury secondary to cerebral syphilitic gumma.
Patient was
stabilised in ED and treated with benzathine penicillin.
Patients with tertiary syphilis poses risk for neurological
complications like, focal neurological deficits and convulsions rhabdomyolysis.
The incidence of tertiary syphilis has
declined in developed countries, but untreated cases still pose a risk for such rare manifestations.
Early recognition and
appropriate management in ED are crucial to prevent severe systemic complications in these patients.
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