Ruano AJM, Nájera RSE, Camacho FL, Cordero BR, Guerrero HM, Vázquez JL

Language: Spanish
References: 5
Page: 279-281
PDF size: 776.22 Kb.

ABSTRACT

Systemic cystic angiomatosis (SCA) is a benign and poorly known condition, characterized by multiple cystic bone, visceral, and soft tissue lesions. Bone lesions, typically in long bones, are usually asymptomatic. Diagnosis is made by exclusion, using clinical, radiological, and non-specific histopathological findings. Treatment varies depending on the location of the bone cysts, while surgical resection is recommended for visceral and soft tissue lesions. This pathology can be mistaken for systemic metastatic activity.

REFERENCES

1. Fernández I, Galbe M, Alvarez C. Angiomatosis quística. An EspPediatr. 2000; 52 (4): 389-391.

2. Almoguera A, Fraga J, Pareja JA, García M. Pathological hip fractureof pediatric age. Revision of the cystic angiomatosis of the bone. ActaOrtop Mex. 2019; 33 (1): 46-49.

3. García-de Quevedo D, Loring P, Méndez L. Angiomatosis quísticaesquelética: a propósito de un caso. Rev Esp Cir Osteoart. 1995; 30:323-326.

4. Paseiro G, Duran H, García J, Bellon J. Angiomatosis quística exclusivadel abdomen sin afectación ósea o de partes blandas. Med Clin (Barc).2008; 131 (6): 238-239.

5. Najm A, Soltner-Neel E, Le Goff B, Guillot P, Maugars Y, BerthelotJM. Cystic angiomatosis, a heterogeneous condition: four newcases and a literature review. Medicine (Baltimore). 2016; 95(43): e5213.