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1.
Article de Anglais | WPRIM | ID: wpr-1003458

RÉSUMÉ

Objective@#To describe a rare case of lipofibromatosis presenting as a head and neck mass in a 6-year-old child.@*Method@#Design: Case Report Setting: Tertiary Public General Hospital Patient: One @*Result@#A six-year-old male child admitted with a large right head and neck region mass underwent complete excision of a possible soft tissue neoplasm following investigations which included Fine Needle Aspiration Cytology, Ultrasonography and Computed Tomography. Histopathological examination yielded lipofibromatosis, a very rare lesion with a distinctive fibrofatty pattern. The patient was well with no recurrence after three months of follow up.@*Conclusion@#Although lipofibromatosis is a rare lesion in children and has a predilection for distal extremities, it may also present as a mass in the head and neck area. Complete surgical excision is feasible and is the only treatment option available for this rare lesion

2.
Article de Anglais | WPRIM | ID: wpr-820090

RÉSUMÉ

Cysticercosis is a condition that occurs when man is infected with larvae of Taenia solium. Oral cysticercosis is a rare event, and it represents difficulty in clinical diagnosis. A case of oral cysticercosis in 11 year old girl is presented which complained of painless swelling for 6 months. A FNAC was performed which revealed bluish pink fibrillary material and interspersed nuclei and fragments of wall of larvae. Patient was treated with antihelminthic.


Sujet(s)
Enfant , Femelle , Humains , Albendazole , Utilisations thérapeutiques , Antiprotozoaires , Utilisations thérapeutiques , Cytoponction , Cysticercose , Diagnostic , Traitement médicamenteux , Lèvre , Parasitologie , Anatomopathologie , Résultat thérapeutique
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