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掌腱膜纤维瘤病(杜普伊特伦挛缩症)。43例的超微结构和酶组织化学研究。

Palmar fibromatosis (Dupuytren's contracture). Ultrastructural and enzyme histochemical studies of 43 cases.

作者信息

Iwasaki H, Müller H, Stutte H J, Brennscheidt U

出版信息

Virchows Arch A Pathol Anat Histopathol. 1984;405(1):41-53. doi: 10.1007/BF00694924.

DOI:10.1007/BF00694924
PMID:6150573
Abstract

Forty three cases of palmar fibromatosis were studied by light and electron microscopy, enzyme histochemistry, and ultrastructural immunohistochemistry. By electron microscopy most of the cells composing the nodules in both the proliferative and the involutional stages were identical to myofibroblasts. The myofibroblasts in the involutional nodules often possessed microfilament aggregates probably representing contraction of micro(actin)filaments in the cytoplasm. The proliferative nodules revealed small perivascular haemorrhages and haemosiderin deposits accompanied by accumulation of macrophages and some lymphocytes; these inflammatory cells possibly secrete a certain growth factor inducing proliferation of genetically abnormal fibroblasts and myofibroblasts. Diaminopeptidase IV was detected in myofibroblasts and fibroblasts by enzyme histochemistry and ultrastructural immunohistochemistry; the enzyme may play a role in the metabolism of intercellular substances. Some perivascular mesenchymal cells, interpreted as variants of myofibroblasts, had moderate activity of alkaline phosphatase.

摘要

对43例掌腱膜纤维瘤病进行了光镜、电镜、酶组织化学及超微结构免疫组织化学研究。电镜下,增殖期和消退期结节中的大多数细胞均与肌成纤维细胞相同。消退期结节中的肌成纤维细胞常含有微丝聚集体,可能代表细胞质中微(肌动蛋白)丝的收缩。增殖期结节可见小的血管周围出血和含铁血黄素沉积,伴有巨噬细胞和一些淋巴细胞聚集;这些炎性细胞可能分泌某种生长因子,诱导基因异常的成纤维细胞和肌成纤维细胞增殖。通过酶组织化学和超微结构免疫组织化学在肌成纤维细胞和成纤维细胞中检测到二肽基肽酶IV;该酶可能在细胞间物质代谢中起作用。一些血管周围间充质细胞被解释为肌成纤维细胞的变体,具有中等活性的碱性磷酸酶。

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Palmar fibromatosis (Dupuytren's contracture). Ultrastructural and enzyme histochemical studies of 43 cases.掌腱膜纤维瘤病(杜普伊特伦挛缩症)。43例的超微结构和酶组织化学研究。
Virchows Arch A Pathol Anat Histopathol. 1984;405(1):41-53. doi: 10.1007/BF00694924.
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引用本文的文献

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WT1 expression is increased in primary fibroblasts derived from Dupuytren's disease tissues.在源自杜普伊特伦挛缩症组织的原代成纤维细胞中,WT1表达增加。
J Cell Commun Signal. 2015 Dec;9(4):347-52. doi: 10.1007/s12079-015-0293-7. Epub 2015 Jun 30.
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Dupuytren's: a systems biology disease.掌腱膜挛缩症:一种系统生物学疾病。
Arthritis Res Ther. 2011;13(5):238. doi: 10.1186/ar3438. Epub 2011 Sep 12.
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Periostin differentially induces proliferation, contraction and apoptosis of primary Dupuytren's disease and adjacent palmar fascia cells.

本文引用的文献

1
RESULTS OF WIDE EXCISION OF THE PALMAR FASCIA FOR DUPUYTREN'S CONTRACTURE: SPECIAL REFERENCE TO FACTORS WHICH ADVERSELY AFFECT PROGNOSIS.掌腱膜广泛切除治疗Dupuytren挛缩症的结果:特别提及对预后产生不利影响的因素。
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Immunocytochemical demonstration of intracytoplasmic alkaline phosphatase in HeLa TCRC-1 cells.
骨膜蛋白可差异诱导原发性掌腱膜挛缩症及相邻掌侧筋膜细胞的增殖、收缩和凋亡。
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Beta-catenin overexpression in Dupuytren's disease is unrelated to disease recurrence.β-连环蛋白在掌腱膜挛缩症中的过表达与疾病复发无关。
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Investigation of proteinases in the digestive tract using 4-methoxy-2-naphthylamine (MNA) substrates.使用4-甲氧基-2-萘胺(MNA)底物对消化道中的蛋白酶进行研究。
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Immunohistochemical localization of dipeptidyl aminopeptidase IV in rat kidney, liver, and salivary glands.二肽基肽酶IV在大鼠肾脏、肝脏和唾液腺中的免疫组织化学定位
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7
Infantile digital fibromatosis. Identification of actin filaments in cytoplasmic inclusions by heavy meromyosin binding.婴儿指纤维瘤病。通过重酶解肌球蛋白结合鉴定细胞质内含物中的肌动蛋白丝。
Cancer. 1983 Nov 1;52(9):1653-61. doi: 10.1002/1097-0142(19831101)52:9<1653::aid-cncr2820520918>3.0.co;2-c.
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Infantile digital fibromatosis. Ultrastructural, histochemical, and tissue culture observations.婴儿指纤维瘤病。超微结构、组织化学及组织培养观察
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Enzymehistochemical staining of T mu lymphocytes for glycyl-proline-4-methoxy-beta-naphthylamide-peptidase (DAP IV).针对甘氨酰脯氨酸-4-甲氧基-β-萘酰胺肽酶(DAP IV)对Tμ淋巴细胞进行酶组织化学染色。
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The new lead citrate method for the ultracytochemical demonstration of activity of non-specific alkaline phosphatase (orthophosphoric monoester phosphohydrolase).用于超细胞化学显示非特异性碱性磷酸酶(正磷酸单酯磷酸水解酶)活性的新型柠檬酸铅法。
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