Velter C, Lipsker D
Clinique dermatologique, hôpitaux universitaires de Strasbourg, faculté de médecine, université de Strasbourg, 1, place de l'Hôpital, 67091 Strasbourg, France.
Clinique dermatologique, hôpitaux universitaires de Strasbourg, faculté de médecine, université de Strasbourg, 1, place de l'Hôpital, 67091 Strasbourg, France.
Rev Med Interne. 2016 Nov;37(11):743-750. doi: 10.1016/j.revmed.2016.05.008. Epub 2016 Jun 16.
Panniculitis is an inflammation of the subcutaneous fat. Skin biopsy plays a critical role in the differential diagnosis of panniculitis. The most common approach to diagnosis relies on the differentiation between predominantly septal or lobular panniculitis, followed by the distinction between lesions with and without vasculitis. It is also very important to submit a part of the skin biopsy for microbiological analysis and for T-cell clonal expansion if T-cell lymphoma is suspected. Erythema nodosum, the most frequent septal panniculitis, has many causes and in its typical clinical presentation, does not require skin biopsy. In other panniculitis, diagnosis is based on the integration of the clinical and histological data, which renders a deep cutaneous biopsy necessary. Periarteritis nodosa, a septal panniculitis with vasculitis characterized by subcutaneous nodules and livedo racemosa, can be associated with systemic involvement. Nodular thrombophlebitis needs search for associated coagulopathy, Behçet's disease, periarteritis nodosa or Buerger's disease. Lobular panniculitis are classified according to the nature of cells present in the inflammatory infiltrate. If there is a lymphocytic infiltration, lupus panniculitis is difficult to differentiate from subcutaneous panniculitis-like T-cell lymphoma. If there are histiocytes, it can be a sarcoidosis, a cytophagic histiocytic panniculitis or, in newborn, a subcutaneous fat necrosis. Neutrophilic panniculitis needs careful clinic-pathologic correlation. Treatment of panniculitis can be challenging and is based on the histopathological findings. Frequently, the precise cause of panniculitis cannot be established from the outset, so it is important to follow-up patients and not hesitate to repeat the skin biopsy.
脂膜炎是皮下脂肪的炎症。皮肤活检在脂膜炎的鉴别诊断中起着关键作用。最常见的诊断方法是区分主要为间隔性或小叶性脂膜炎,然后区分有无血管炎的病变。如果怀疑是T细胞淋巴瘤,将皮肤活检的一部分送去进行微生物分析和T细胞克隆扩增检查也非常重要。结节性红斑是最常见的间隔性脂膜炎,病因众多,在其典型临床表现下,不需要进行皮肤活检。在其他脂膜炎中,诊断基于临床和组织学数据的综合,这使得进行深部皮肤活检成为必要。结节性多动脉炎是一种伴有血管炎的间隔性脂膜炎,其特征为皮下结节和网状青斑,可伴有全身受累。结节性血栓性静脉炎需要排查相关的凝血病、白塞病、结节性多动脉炎或血栓闭塞性脉管炎。小叶性脂膜炎根据炎症浸润中存在的细胞性质进行分类。如果有淋巴细胞浸润,狼疮性脂膜炎很难与皮下脂膜炎样T细胞淋巴瘤区分开来。如果有组织细胞,则可能是结节病、噬血细胞性组织细胞性脂膜炎,或者在新生儿中,是皮下脂肪坏死。中性粒细胞性脂膜炎需要仔细的临床病理相关性分析。脂膜炎的治疗可能具有挑战性,且基于组织病理学结果。通常,脂膜炎的确切病因从一开始就无法确定,因此对患者进行随访并毫不犹豫地重复皮肤活检很重要。