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J Pediatr Hematol Oncol ; 44(2): e450-e452, 2022 Mar 01.
Artículo en Inglés | MEDLINE | ID: mdl-35200222

RESUMEN

In people with sickle cell disease (SCD), oral abscesses are concerning clinical conditions and carry a high risk of postoperative sickle cell complications. We present an unusual case of a 14-year-old girl with SCD whose initial presentation of facial swelling, headaches, jaw pain, and paresthesia mimicked an odontogenic abscess. She was diagnosed with vaso-occlusive crisis in the mandibular bone and successfully managed noninvasively. This is among the youngest cases of paresthesia in the lower lip in SCD, which provided a clue that postponing invasive aspiration or biopsy was possible under empiric antibiotics and close observation.


Asunto(s)
Anemia de Células Falciformes , Enfermedades Maxilomandibulares , Absceso/diagnóstico , Absceso/etiología , Adolescente , Anemia de Células Falciformes/complicaciones , Femenino , Humanos , Mandíbula , Dolor/diagnóstico , Dolor/etiología , Parestesia/complicaciones
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