Goto Keisuke, Ishizaki Sumiko, Tanese Keiji, Oshitani Yoshimi, Kaku Yo, Kaneko Rie, Takama Hiromichi, Ishikawa Misawo, Tanaka Masaru
*Department of Diagnostic Pathology, Kainan Hospital, Yatomi, Japan; †Department of Dermatology, Tokyo Women's Medical University Medical Center East, Tokyo, Japan; ‡Department of Dermatology, Keio University School of Medicine, Tokyo, Japan; §Department of Dermatology, Kainan Hospital, Yatomi, Japan; ¶Department of Dermatology, Kyoto University Graduate School of Medicine, Kyoto, Japan; ‖Department of Dermatology, Nikko Memorial Hospital, Muroran, Japan; and **Takama Dermatology Clinic, Kasugai, Japan.
Am J Dermatopathol. 2016 Feb;38(2):124-30. doi: 10.1097/DAD.0000000000000414.
Nonepisodic angioedema with eosinophilia (NEAE) is a rare condition characterized with monoepisodic angioedema, a nonfebrile state, eosinophilia, normal serum IgM levels, and lack of internal organ involvement. The histology of this disease is not yet well known. The purpose of this study was to characterize the histopathologic features of NEAE. Twelve cases of clinically confirmed NEAE were retrieved from 6 institutions, and these cases were reviewed regarding the clinical data and histopathology, particularly regarding granulomatous lesions. The authors demonstrated that the histology of NEAE can be classified into 3 patterns that of eosinophilic granulomatous panniculitis (7/12 cases), eosinophilic dermatitis without granuloma formation (3/12 cases), and invisible dermatosis (2/12 cases). Six of the 7 granulomatous cases showed the characteristic eosinophilic granulomatous lesions containing individual necrotic adipocytes with membranous fat changes, which could be a differential clue to the diagnosis of NEAE. Review of the previously reported cases (n = 37) revealed that the histological classification could be adaptable to these reported cases. The authors should recognize the histological variation of NEAE and distinguish it from the histological mimickers, including eosinophilic granulomatosis with polyangiitis, erythema nodosum, hypereosinophilic syndrome, and episodic angioedema with eosinophilia.
非周期性嗜酸性粒细胞增多性血管性水肿(NEAE)是一种罕见疾病,其特征为单次发作性血管性水肿、无发热状态、嗜酸性粒细胞增多、血清IgM水平正常且无内脏器官受累。这种疾病的组织学情况尚不为人所知。本研究的目的是描述NEAE的组织病理学特征。从6家机构检索出12例临床确诊的NEAE病例,并对这些病例的临床资料和组织病理学进行回顾,尤其关注肉芽肿性病变。作者证明,NEAE的组织学可分为3种类型:嗜酸性粒细胞性肉芽肿性脂膜炎(7/12例)、无肉芽肿形成的嗜酸性粒细胞性皮炎(3/12例)和隐匿性皮肤病(2/12例)。7例肉芽肿性病例中有6例显示出特征性的嗜酸性粒细胞性肉芽肿病变,包含单个坏死脂肪细胞及膜性脂肪改变,这可能是诊断NEAE的鉴别线索。对先前报道的病例(n = 37)进行回顾发现,组织学分类也适用于这些报道的病例。作者应认识到NEAE的组织学变异,并将其与组织学上的模仿者区分开来,包括嗜酸性粒细胞性肉芽肿性多血管炎、结节性红斑、高嗜酸性粒细胞综合征和周期性嗜酸性粒细胞增多性血管性水肿。