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[Giant and ulcerated juvenile xanthogranuloma: an atypical presentation in infants]. / Xantogranuloma juvenil gigante y ulcerado: una presentación atípica en lactantes.
Guelfand Warnken, Sofia; Fajre Wipe, Ximena; Suarez Aldunate, Claudia; Agüero Ureta, Rosario; Castro Méndez, Alex.
Afiliación
  • Guelfand Warnken S; Universidad del Desarrollo, Santiago, Chile.
  • Fajre Wipe X; Universidad del Desarrollo, Santiago, Chile.
  • Suarez Aldunate C; Universidad del Desarrollo, Santiago, Chile.
  • Agüero Ureta R; University of Southern California, Los Angeles, USA.
  • Castro Méndez A; Facultad de Medicina, Universidad del Desarrollo, Santiago, Chile.
Andes Pediatr ; 94(5): 646-651, 2023 Oct.
Article en Es | MEDLINE | ID: mdl-37975698
ABSTRACT
Giant Juvenile Xanthogranuloma (GJXG) corresponds to an infrequent variant of Juvenile Xantho- granuloma (JXG) and is characterized by a lesion larger than 2 cm in diameter. It usually presents as a plaque but infrequently, presents as an ulcerated nodule.

OBJECTIVE:

To report two cases of atypical presentation of GJXG, highlighting the importance of considering them in the differential diagnosis of large, ulcerated tumors in infants. CLINICAL CASES Case 1 A 4-month-old healthy male infant presented with a rapid and progressive growing left inguinal nodule, present since 2 months of age. At physical examination he presented with a 2.6 cm indurated erythematous nodule with central ulceration. Histological study of an incisional biopsy was compatible with JXG. Ophthalmologic involvement was ruled out. Because of functional impairment and parents worry complete surgical removal was performed. The patient had favorable evolution without local recurrence at 4 years of follow-up. Case 2 A 6-month-old healthy male infant presented with a 2.4 cm scapular crusted nodule of rapid and progressive growth, present since birth. Histological study of an incisional biopsy confirmed JXG. Ophthalmologic involvement was ruled out. After 18 months of periodic clinical follow-up, there was a progressive reduction in size of the lesion.

CONCLUSIONS:

The cases presented highlight the importance of considering JXG in the differential diagnosis of large, ulcerated tumors in infants. When encountered to atypical JXG presentations, histologic studies help to confirm the diagnosis. Given the favorable prognosis of this diagnosis, periodic clinical follow-up is advised; in exceptional cases, surgical or ablative treatments may be considered.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Xantogranuloma Juvenil / Neoplasias Límite: Humans / Infant / Male Idioma: Es Revista: Andes Pediatr Año: 2023 Tipo del documento: Article País de afiliación: Chile

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Xantogranuloma Juvenil / Neoplasias Límite: Humans / Infant / Male Idioma: Es Revista: Andes Pediatr Año: 2023 Tipo del documento: Article País de afiliación: Chile