Schmidt Birgitta A R, El Zein Sophie, Cuoto Javier, Al-Ibraheemi Alyaa, Liang Marilyn G, Paltiel Harriet J, Anderson Megan E, Labow Brian I, Upton Joseph, Fishman Steven J, Mulliken John B, Greene Arin K, Warman Mathew L, Kozakewich Harry
Department of Pathology, Boston Children's Hospital and Harvard Medical School, Boston, MA.
Department of Pathology, Institute Curie, Paris, France.
Am J Dermatopathol. 2021 Dec 1;43(12):e181-e184. doi: 10.1097/DAD.0000000000001963.
Verrucous venous malformation (VVM), previously called "verrucous hemangioma," typically involves the dermis and the subcutaneous fat. We have encountered patients with VVM confined to the hypodermis.
During a nearly 20-year period, 13 patients, aged 2-17 years, presented with a subcutaneous mass in the limb without clinically obvious epidermal alterations. Consequently, operative excisions did not include the skin.
Histopathologically, the specimens were composed of blood-filled channels with morphologic characteristics of capillaries and veins that infiltrated adipose tissue. Aggregates often formed nodules with variable fibrosis and a component of large and radially oriented vessels. A diagnosis of VVM was supported by endothelial immunopositivity for GLUT-1 (25%-75% immunopositive channels in 16/16 specimens); D2-40 (1%-25% channels in 14/15 specimens); and Prox-1 (1%-50% of channels in 14/16 specimens). A MAP3K3 mutation was identified by droplet digital PCR in 3 of the 6 specimens.
Diagnosis of VVM in this uncommon location is challenging because of absence of epidermal changes and lack of dermal involvement. Imaging is not pathognomonic, and mimickers are many. Appropriate immunohistochemical stains and molecular analysis contribute to the correct diagnosis.
疣状静脉畸形(VVM),以前称为“疣状血管瘤”,通常累及真皮和皮下脂肪。我们遇到了局限于皮下组织的VVM患者。
在近20年的时间里,13例年龄在2至17岁的患者,其肢体出现皮下肿块,临床上无明显的表皮改变。因此,手术切除未包括皮肤。
组织病理学上,标本由充满血液的通道组成,这些通道具有毛细血管和静脉的形态特征,并浸润脂肪组织。聚集物常形成结节,伴有不同程度的纤维化以及大的、呈放射状排列的血管成分。VVM的诊断得到以下支持:GLUT-1内皮免疫阳性(16/16标本中25%-75%的通道免疫阳性);D2-40(14/15标本中1%-25%的通道);以及Prox-1(14/16标本中1%-50%的通道)。在6个标本中的3个通过液滴数字PCR鉴定出MAP3K3突变。
由于没有表皮改变且未累及真皮,在这个不常见部位诊断VVM具有挑战性。影像学检查不具有特异性,且有许多类似疾病。适当的免疫组化染色和分子分析有助于正确诊断。