2020
DOI: 10.1016/j.ad.2020.07.004
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Xantogranuloma juvenil: una entidad con amplio espectro clínico

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Cited by 29 publications
(13 citation statements)
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“…11 It is a benign disease and, in general, does not require treatment; however, if systemic involvement is present, treatment with corticosteroids and vinblastine may be indicated. 12 In case 2, the patient had associated neutropenia. Based on this, secondary causes were initially looked for, such as infections, mainly of the TORCH group, which manifest as hepatosplenomegaly, anemia, thrombocytopenia, and the blueberry muffin syndrome appearance with bluish subcutaneous nodules.…”
Section: Discussionmentioning
confidence: 99%
“…11 It is a benign disease and, in general, does not require treatment; however, if systemic involvement is present, treatment with corticosteroids and vinblastine may be indicated. 12 In case 2, the patient had associated neutropenia. Based on this, secondary causes were initially looked for, such as infections, mainly of the TORCH group, which manifest as hepatosplenomegaly, anemia, thrombocytopenia, and the blueberry muffin syndrome appearance with bluish subcutaneous nodules.…”
Section: Discussionmentioning
confidence: 99%
“…11 Se trata de una patología benigna y, en general, no requiere tratamiento, sin embargo, si se presenta compromiso sistémico, se puede utilizar un esquema de corticoides y vinblastina. 12 En el caso 2 el paciente presentó neutropenia asociada. Esto motivó inicialmente la búsqueda de causas secundarias, como infecciones, principalmente del grupo TORCH, que se manifiestan con hepatoesplenomegalia, anemia, trombocitopenia y el aspecto blueberry muffin syndrome con nódulos subcutáneos azulados.…”
Section: Figura 3 Anatomía Patológica Del Caso Número 2 Se Puede Obse...unclassified
“…Diagnosis is usually clinical, but diagnostic skin biopsy is recommended in case of multiple lesions to rule out other pathologic processes. Histology shows dense, well-demarcated dermal lymphohistiocytic infiltration interlaced with giant cells, and immunohistochemistry positive for macrophage markers (CD68, CD163, KiM1P, anti-FXIIIa, vimentin and anti-CD4) and negative for S100, CD1a and CD207, specific for Langerhans cells [2][3][4] . Differential diagnosis, mainly in multiple forms, includes: Langerhans cell histiocytosis, other non-Langerhans cell histiocytosis (cephalic histiocytosis, generalized eruptive histiocytoma, giant cell reticulohistiocytoma), urticaria pigmentosa, tuberous xanthomas, dermatofibroma, angiomas, nevus, molluscum contagiosum and pyogenic granuloma 5 .…”
Section: Main Textmentioning
confidence: 99%
“…Considering that extracutaneous involvement is rare, there is no consensus on the need for additional tests in patients with no associated systemic symptoms. Some authors advocate neuro-ophthalmologic evaluation and the performance of complementary tests, such as blood analysis with hemogram and liver profile and additional imaging tests, in high-risk cases: new diagnosis, multiple skin lesions, age younger than 2 years, or signs and symptoms suggestive of visceral involvement 2,3,6 .…”
mentioning
confidence: 99%