Atypical congenital toxoplasmosis presenting with neonatal jaundice and central nervous system involvement: a case report and therapeutic challenges to limited access to first-line anti-toxoplasma medications - Takeaways - MDSpire

Atypical congenital toxoplasmosis presenting with neonatal jaundice and central nervous system involvement: a case report and therapeutic challenges to limited access to first-line anti-toxoplasma medications

  • By

  • Li Wang

  • Kaiwei Ding

  • Shuai Yu

  • Zheng Guo

  • Yongjiao Wang

  • Lingkong Zeng

  • Wenhao Yuan

  • June 25, 2026

  • 0 min

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  • 1

    Congenital toxoplasmosis can present with isolated neonatal jaundice, which may delay diagnosis and complicate treatment.

  • 2

    A 9-day-old male infant with jaundice was diagnosed with congenital toxoplasmosis after positive serological tests and T. gondii DNA detection.

  • 3

    The infant exhibited subclinical chorioretinitis, cerebral edema, and auditory dysfunction, highlighting the diverse manifestations of congenital toxoplasmosis.

  • 4

    Initial treatment with azithromycin and trimethoprim-sulfamethoxazole showed no improvement, necessitating a switch to standard therapy.

  • 5

    After starting pyrimethamine, sulfadiazine, and folinic acid, the patient showed rapid clinical improvement and resolution of brain lesions.

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