Slack Jonathan C, Sanchez-Glanville Carlos, Steele MacGregor, Wong Andrew L, Bründler Marie-Anne
Departments of Pathology and Laboratory Medicine.
Pediatric General Surgery.
J Pediatr Hematol Oncol. 2018 May;40(4):307-311. doi: 10.1097/MPH.0000000000001088.
Angiomatoid fibrous histiocytoma (AFH) is a rare soft tissue tumor that typically presents in children and young adults. Occurrence outside of the extremities and the head and neck region is exceedingly rare. We report the case of a 9-year-old boy who presented with recurrent retroperitoneal hemorrhage initially thought to be a manifestation of an underlying bleeding disorder. After comprehensive diagnostic work-up, including multiple negative biopsies, the patient underwent surgical resection of an extensively hemorrhagic intramuscular mass and to date remains well. Pathologic examination confirmed AFH with EWSR1 gene rearrangement. This first documented report of an AFH in a retroperitoneal location in a child highlights the diagnostic difficulties and clinical challenges of AFH arising in an atypical location.
血管样纤维组织细胞瘤(AFH)是一种罕见的软组织肿瘤,多见于儿童和青年。发生于四肢及头颈部以外部位极为罕见。我们报告一例9岁男孩,最初表现为反复的腹膜后出血,最初认为是潜在出血性疾病的表现。经过全面的诊断检查,包括多次活检阴性,患者接受了广泛出血性肌内肿块的手术切除,至今情况良好。病理检查证实为伴有EWSR1基因重排的AFH。这是首次报道儿童腹膜后部位的AFH,突出了非典型部位AFH的诊断困难和临床挑战。