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Moyamoya disease presenting with tubular dysfunction in a child: pitfalls in diagnosing an atypical hyponatremic-hypertensive syndrome.
Conte, Maria Luisa; La Scola, Claudio; Mencarelli, Francesca; Filippini, Beatrice; Fabbri, Elena; Ragnoni, Valentina; Ravaioli, Elisa; Pasini, Andrea; Vergine, Gianluca.
Afiliação
  • Conte ML; Department of Pediatrics, Infermi Hospital, Viale Settembrini, 2, 47900, Rimini, Italy.
  • La Scola C; Pediatric Nephrology and Dialysis, Pediatric Unit, IRCCS AziendaOspedaliero-Universitaria Di Bologna, Bologna, Italy.
  • Mencarelli F; Pediatric Nephrology and Dialysis, Pediatric Unit, IRCCS AziendaOspedaliero-Universitaria Di Bologna, Bologna, Italy.
  • Filippini B; Department of Pediatrics, Infermi Hospital, Viale Settembrini, 2, 47900, Rimini, Italy.
  • Fabbri E; Department of Pediatrics, Infermi Hospital, Viale Settembrini, 2, 47900, Rimini, Italy.
  • Ragnoni V; Department of Pediatrics, Infermi Hospital, Viale Settembrini, 2, 47900, Rimini, Italy.
  • Ravaioli E; Department of Pediatrics, Infermi Hospital, Viale Settembrini, 2, 47900, Rimini, Italy.
  • Pasini A; Pediatric Nephrology and Dialysis, Pediatric Unit, IRCCS AziendaOspedaliero-Universitaria Di Bologna, Bologna, Italy.
  • Vergine G; Department of Pediatrics, Infermi Hospital, Viale Settembrini, 2, 47900, Rimini, Italy. gianluca.vergine@auslromagna.it.
BMC Pediatr ; 23(1): 227, 2023 05 08.
Article em En | MEDLINE | ID: mdl-37150827
ABSTRACT

BACKGROUND:

Moyamoya disease, a cause of pediatric stroke, has been shown to affect furthermore extra-cranial districts, mostly the kidney arterial site, resulting in steno-occlusive changes. Unilateral renal artery stenosis accounts for 8%-10% out of cases of renovascular hypertension in childhood, however it rarely underlies a hyponatremic-hypertensive syndrome (HHS). CASE PRESENTATION We describe an 18-month-old boy with a recent history of polyuria and polydipsia, who presented an acute febrile gastroenteritis with neurological impairment, severe dehydration, hyponatremia, hypokalemia, kidney tubular dysfunction, and elevated aldosterone and renin even with a normal blood pressure. Fluid and electrolytes correction was performed, with complete recovery. An abdominal ultrasound displayed a smaller right kidney. A brain magnetic resonance and an electroencephalogram did not show any relevant abnormalities. Five months later, the child experienced a left-side hemiparesis after a traumatic concussion, and a severe hypertension. A brain tomography documented a cerebral ischemia. Brain and kidney angiographic studies displayed puff of smoke findings of internal right carotid artery branches and a steno-occlusive pattern of right renal artery, respectively. Hence, moyamoya disease with HHS secondary to unilateral renal artery stenosis was diagnosed. After an unsuccessful antiplatelet and antihypertensive pharmacological treatment, the boy underwent a renal angioplasty and a cerebral STA-MCA bypass (direct superficial temporal artery-to-middle cerebral artery bypass), resulting in a significant improvement of both neurological and kidney disease.

CONCLUSIONS:

Although the association between unilateral renal artery stenosis and HHS has been previously shown, this is the first report of atypical HHS, with hypertension preceded by tubular dysfunction, recognized in the framework of moyamoya disease.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Limite: Child / Humans / Infant / Male Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Limite: Child / Humans / Infant / Male Idioma: En Ano de publicação: 2023 Tipo de documento: Article