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1.
J Cancer Res Ther ; 2020 Jul; 16(3): 661-664
Article | IMSEAR | ID: sea-213678

Résumé

The present case report is a case of peripheral dentinogenic ghost cell tumor (PDGCT), an extremely rare solid benign neoplastic variant of calcifying cystic odontogenic tumor of the gingiva mimicking clinically as pyogenic granuloma, fibroma, peripheral ossifying fibroma, and peripheral giant-cell granuloma. A 24-year-old male reported with painless, firm, solitary, sessile, smooth-surfaced, nonulcerative, nonpulsatile, well-defined swelling measuring ≈12 mm × 9 mm in the interdental gingiva of the teeth #13 and #14 extending to the mucogingival junction. Intraoral periapical radiographic showed a normal trabecular pattern with mild radiolucency without bony expansion, periapical lesion, and resorption of the adjacent teeth. The diagnosis was established by histopathologic examination. Very few cases of this entity have been documented in the literature. The present case report aims to document this rare entity and emphasizes on the fact that histopathological examination of every localized gingival growth should be included in the treatment planning to differentiate with other commonly found lesions

2.
Indian Pediatr ; 2020 Jan; 57(1): 66-67
Article | IMSEAR | ID: sea-199455

Résumé

A retrospective study was conducted including all the childrenwho sustained motorized machine belt entrapment injuries. Sixchildren included in study had mean (SD) Glosgow coma scaleand pediatric trauma score of 5.7 (3.54) and 3.2 (1.21),respectively. Overall mortality and paraplegia rate were 33.3%each. Awareness and legislation both are important to curb thismenace

3.
Indian Pediatr ; 2019 Dec; 55(12): 1087-1088
Article | IMSEAR | ID: sea-199119

Résumé

Background: Neonatal respiratory distress due to coexisting subglosso-palatalmembrane and tongue dermoid has not been reported yet. Case characteristics: Anewborn with respiratory distress having a membrane in the oral cavity. Excision ofmembrane revealed a tongue mass with cleft palate, obstructing the nasopharynxcompletely. Elective ventilation was followed by excision of mass. Outcome: The childwas cured with uneventful course at follow-up of six months. Message: Co-existingcongenital anomalies causing airway obstruction may be missed in presence ofsubglosso-palatal membrane.

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