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斯威特综合征：15例的组织学和免疫组织化学研究

Sweet's syndrome: histological and immunohistochemical study of 15 cases.

作者信息

Going J J, Going S M, Myśkoẃ M W, Beveridge G W

出版信息

J Clin Pathol. 1987 Feb;40(2):175-9. doi: 10.1136/jcp.40.2.175.

DOI:10.1136/jcp.40.2.175
PMID:3546396
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1140863/
Abstract

Conventional histology and immunoperoxidase staining for fibrin, immunoglobulins, and complement components were used to look for evidence of cutaneous vasculitis and immune complex deposition in Sweet's syndrome. These features were not identified in any of the 15 cases studied. The lack of any vasculitis emphasises the distinctive character of Sweet's syndrome when compared with certain spontaneous and experimentally induced inflammatory skin lesions, and may imply a similarly distinctive pathogenesis.

摘要

采用传统组织学方法以及针对纤维蛋白、免疫球蛋白和补体成分的免疫过氧化物酶染色，来寻找Sweet综合征中皮肤血管炎和免疫复合物沉积的证据。在所研究的15例病例中均未发现这些特征。与某些自发性和实验性诱导的炎症性皮肤病变相比，缺乏任何血管炎强调了Sweet综合征的独特性质，并且可能暗示其发病机制同样独特。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6889/1140863/d6a9fbf35a1d/jclinpath00322-0054-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6889/1140863/1732b933c4f0/jclinpath00322-0052-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6889/1140863/c5018b2bf8ba/jclinpath00322-0052-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6889/1140863/b044c959546a/jclinpath00322-0053-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6889/1140863/d2f725395302/jclinpath00322-0053-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6889/1140863/d6a9fbf35a1d/jclinpath00322-0054-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6889/1140863/1732b933c4f0/jclinpath00322-0052-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6889/1140863/c5018b2bf8ba/jclinpath00322-0052-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6889/1140863/b044c959546a/jclinpath00322-0053-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6889/1140863/d2f725395302/jclinpath00322-0053-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6889/1140863/d6a9fbf35a1d/jclinpath00322-0054-a.jpg

相似文献

1
Sweet's syndrome: histological and immunohistochemical study of 15 cases.斯威特综合征：15例的组织学和免疫组织化学研究
J Clin Pathol. 1987 Feb;40(2):175-9. doi: 10.1136/jcp.40.2.175.
2
Histiocytes in Sweet's syndrome.斯威特综合征中的组织细胞。
Br J Dermatol. 1991 Apr;124(4):348-53. doi: 10.1111/j.1365-2133.1991.tb00595.x.
3
[Sweet's acute febrile neutrophilic dermatosis].
Vestn Dermatol Venerol. 1988(8):58-61.
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Arch Dermatol. 1989 Aug;125(8):1101-4.
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6
[Sweet's syndrome associated with myelodysplastic syndrome].
Rinsho Ketsueki. 1989 May;30(5):764-7.
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Acute febrile neutrophilic dermatosis in childhood (Sweet's syndrome).儿童急性发热性嗜中性皮病（斯威特综合征）。
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8
Sweet's syndrome with lung involvement.伴有肺部受累的Sweet综合征。
Am Rev Respir Dis. 1991 Jan;143(1):177-9. doi: 10.1164/ajrccm/143.1.177.
9
[Sweet's syndrome (acute febrile neutrophilic dermatosis)].[斯威特综合征（急性发热性嗜中性皮病）]
Vestn Dermatol Venerol. 1981(10):35-7.
10
Sweet's syndrome in chronic lymphocytic leukemia.慢性淋巴细胞白血病中的Sweet综合征。
Acta Biomed Ateneo Parmense. 1984;55(3-4):197-8.

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A case of seronegative longitudinally extensive transverse myelitis with possible neuro sweet disease.一例可能为神经白塞病的血清阴性纵向广泛横贯性脊髓炎病例。
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本文引用的文献

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Studies on the mechanism of the Shwartzman-phenomenon; evidence for the participation of polymorphonuclear leucocytes in the phenomenon.施瓦茨曼现象的机制研究；多形核白细胞参与该现象的证据。
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Neutrophilic dermal infiltrates in granulocytopenic patients with acute leukemia.急性白血病粒细胞减少患者的中性粒细胞性皮肤浸润
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[Sweet syndrome in chronic myeloid leukemia].
Klin Wochenschr. 1989 May 2;67(9):506-10. doi: 10.1007/BF01721678.
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Acute febrile neutrophilic dermatosis (Sweet's syndrome) and myeloproliferative disorders.
Cancer. 1983 Apr 15;51(8):1518-26. doi: 10.1002/1097-0142(19830415)51:8<1518::aid-cncr2820510827>3.0.co;2-u.
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Neutrophilic dermatosis of myeloproliferative disorders. Atypical forms of pyoderma gangrenosum and Sweet's syndrome associated with myeloproliferative disorders.骨髓增殖性疾病的嗜中性皮病。与骨髓增殖性疾病相关的坏疽性脓皮病和Sweet综合征的非典型形式。
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Sweet's syndrome and pyoderma gangrenosum associated with ulcerative colitis.与溃疡性结肠炎相关的Sweet综合征和坏疽性脓皮病。
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