[Angiomatoid fibrous histiocytoma in children: 6 cases]

Ann Dermatol Venereol. 2015 Oct;142(10):541-8. doi: 10.1016/j.annder.2015.07.007. Epub 2015 Sep 9.
[Article in French]

Abstract

Background: Angiomatoid fibrous histiocytoma (AFH) is a soft-tissue tumour of uncertain differentiation most often arising in the extremities of children and young adults. AFH is a little-known neoplasm and its rarity may result in it being misdiagnosed as either a reactive lesion or a benign or higher-grade tumour. We report 6 cases of AFH in children and we review the clinicopathological and molecular features of this neoplasm published in the literature.

Patients and methods: The children (aged 4 to 16 years) presented a single nodule involving the forearm (4/6), the trunk or the buttock, and all 5 nodules appeared spontaneously. Microscopic examination revealed well-circumscribed nodular lesions comprising a fibrous pseudo-capsule, haemorrhagic non-endothelial-lined pseudocystic spaces, and sheets of spindle and ovoid cells with dense surrounding lymphoplasmacytic infiltrate. Tumours were positive for desmin, CD68, CD99 and smooth-muscle actin markers. A fusion gene (EWSR1-ATF1) was found in the 3 cases in which molecular investigation was performed.

Discussion: In our series, a diagnosis of AFH had in no event been evoked after clinical examination and radiological investigation. The diagnosis was based in all cases on recognition of characteristic features during histological examination and it was confirmed in 3 cases by the recognition of fusion genes. Complete excision with wide margins allowed complete cure in all cases, supporting a good prognosis of AFH, although long-term follow-up is still mandatory to rule out relapse or metastases, which although rare, are responsible for fatal cases. To avoid unnecessary surgery in patients with AFH, an ultrasound core-needle biopsy should be performed as a first step in order to provide precise diagnosis enabling complete excision to be performed, with the margins being decided in multidisciplinary meetings involving teams specialised in soft-tissue tumours.

Keywords: ATF1; Angiomatoid fibrous histiocytoma; Children; EWSR1; Enfant; Histiocytome fibreux angiomatoïde; Sarcoma; Sarcome.

Publication types

  • Review

MeSH terms

  • 12E7 Antigen
  • Actins / analysis
  • Adolescent
  • Antigens, CD / analysis
  • Antigens, Differentiation, Myelomonocytic / analysis
  • Biomarkers, Tumor / analysis*
  • Biomarkers, Tumor / genetics
  • Biopsy, Needle / methods
  • Cell Adhesion Molecules / analysis
  • Child
  • Child, Preschool
  • Desmin / analysis
  • Female
  • Histiocytoma, Malignant Fibrous / chemistry
  • Histiocytoma, Malignant Fibrous / diagnosis*
  • Histiocytoma, Malignant Fibrous / genetics
  • Histiocytoma, Malignant Fibrous / pathology
  • Histiocytoma, Malignant Fibrous / surgery
  • Humans
  • Male
  • Oncogene Proteins, Fusion / analysis*
  • Oncogene Proteins, Fusion / genetics
  • Prognosis
  • Remission Induction
  • Skin Neoplasms / chemistry
  • Skin Neoplasms / diagnosis*
  • Skin Neoplasms / genetics
  • Skin Neoplasms / pathology
  • Skin Neoplasms / surgery
  • Ultrasonography, Interventional

Substances

  • 12E7 Antigen
  • Actins
  • Antigens, CD
  • Antigens, Differentiation, Myelomonocytic
  • Biomarkers, Tumor
  • CD68 antigen, human
  • CD99 protein, human
  • Cell Adhesion Molecules
  • Desmin
  • EWSR1-ATF1 fusion protein, human
  • Oncogene Proteins, Fusion

Supplementary concepts

  • Histiocytoma, Angiomatoid Fibrous