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伴有梭形细胞分化及肿瘤形成的恶性组织细胞增多症（组织细胞性髓性网状细胞增生症）

Malignant histiocytosis (histiocytic medullary reticulosis) with spindle cell differentiation and tumour formation.

作者信息

Macgillivray J B, Duthie J S

出版信息

J Clin Pathol. 1977 Feb;30(2):120-5. doi: 10.1136/jcp.30.2.120.

DOI:10.1136/jcp.30.2.120
PMID:845260
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC476333/
Abstract

Malignant histiocytosis (histiocytic medullary reticulosis) in a 45-year-old white man is described. Unusual features were presentation as a surgical emergency with signs of obstruction and peritonitis due to an ileal tumour and extensive spindle cell differentiation. Problems in the differential diagnosis of malignant histiocytosis are briefly discussed.

摘要

本文描述了一名45岁白人男性的恶性组织细胞增多症（组织细胞性髓性网状细胞增生症）。其不寻常的特征表现为因回肠肿瘤导致的肠梗阻和腹膜炎体征，作为外科急症就诊，且存在广泛的梭形细胞分化。文中简要讨论了恶性组织细胞增多症鉴别诊断中的问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d927/476333/766cc37f86f5/jclinpath00160-0025-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d927/476333/4dcf7f8bc465/jclinpath00160-0024-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d927/476333/6c67fce6f5b3/jclinpath00160-0024-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d927/476333/5edf4f21d02a/jclinpath00160-0024-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d927/476333/498798b6670b/jclinpath00160-0023-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d927/476333/5171dfd38687/jclinpath00160-0023-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d927/476333/304fcdab20cd/jclinpath00160-0025-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d927/476333/766cc37f86f5/jclinpath00160-0025-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d927/476333/4dcf7f8bc465/jclinpath00160-0024-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d927/476333/6c67fce6f5b3/jclinpath00160-0024-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d927/476333/5edf4f21d02a/jclinpath00160-0024-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d927/476333/498798b6670b/jclinpath00160-0023-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d927/476333/5171dfd38687/jclinpath00160-0023-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d927/476333/304fcdab20cd/jclinpath00160-0025-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d927/476333/766cc37f86f5/jclinpath00160-0025-b.jpg

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Malignant histiocytosis (histiocytic medullary reticulosis) with spindle cell differentiation and tumour formation.伴有梭形细胞分化及肿瘤形成的恶性组织细胞增多症（组织细胞性髓性网状细胞增生症）
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引用本文的文献

1
Villous atrophy with crypt hyperplasia in malignant histiocytosis of the nose.鼻部恶性组织细胞增多症中的绒毛萎缩伴隐窝增生
J Clin Pathol. 1982 Jun;35(6):606-10. doi: 10.1136/jcp.35.6.606.

本文引用的文献

1
Cultural characteristics of malignant histiocytomas and fibrous xanthomas.恶性组织细胞瘤和纤维性黄色瘤的文化特征。 （不过这里原文中的“文化特征”表述可能有误，结合医学内容推测应该是“组织学特征”之类的意思更合理。）
Cancer. 1963 Mar;16:331-44. doi: 10.1002/1097-0142(196303)16:3<331::aid-cncr2820160307>3.0.co;2-f.
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Histiocytic medullary reticulosis.组织细胞性髓性网状细胞增生症
Proc Staff Meet Mayo Clin. 1962 May 9;37:271-83.
3
Autoimmune hemolytic anemia. II. Morphologic observations and clinicopathologic correlations.自身免疫性溶血性贫血。II. 形态学观察及临床病理相关性
Am J Pathol. 1957 May-Jun;33(3):429-57.
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Histiocytic medullary reticulosis.组织细胞性髓性网状细胞增生症
J Pathol Bacteriol. 1956 Jan;71(1):61-71. doi: 10.1002/path.1700710110.
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Histiocytic medullary reticulosis presenting with a leukemic blood picture.呈现白血病血象的组织细胞性髓性网状细胞增生症。
Am J Med. 1969 Aug;47(2):314-7. doi: 10.1016/0002-9343(69)90157-0.
6
Histiocytic medullary reticulosis. Report of 14 cases from Uganda.组织细胞性髓性网状细胞增生症。乌干达14例报告。
Br J Cancer. 1968 Sep;22(3):506-16. doi: 10.1038/bjc.1968.60.
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Rod-like tubular structures in the cytoplasm of histiocytes in "histiocytosis x".
J Pathol Bacteriol. 1968 Jan;95(1):123-6. doi: 10.1002/path.1700950114.
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Lymph node ultrastructure in Hand-Schüller-Christian disease.汉-许-克病中的淋巴结超微结构
Cancer. 1971 Apr;27(4):956-64. doi: 10.1002/1097-0142(197104)27:4<956::aid-cncr2820270431>3.0.co;2-g.
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Malignant histiocytosis: a case of generalized histiocytosis with infiltration of Langerhans' granule-containing histiocytes.
Cancer. 1971 Aug;28(2):467-75. doi: 10.1002/1097-0142(197108)28:2<467::aid-cncr2820280228>3.0.co;2-9.
10
Histiocytic medullary reticulosis. Report of two cases and review of the literature.
Arch Dermatol. 1972 Sep;106(3):319-29. doi: 10.1001/archderm.106.3.319.