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肿瘤性钙化——一种未被认识的疾病。

Tumoral calcinosis--an unrecognized disease.

作者信息

McClatchie S, Bremner A D

出版信息

Br Med J. 1969 Jan 18;1(5637):153-5. doi: 10.1136/bmj.1.5637.142-a.

DOI:10.1136/bmj.1.5637.142-a
PMID:5762276
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1982282/
Abstract

Twenty-six cases of tumoral calcinosis are reported from Kenya. The disease, frequently misdiagnosed, is of unknown origin. It presents as calcified tumours, usually around the hips and buttocks, in muscle and subcutaneous tissue. The tumours are partly solid, partly multiloculated cysts which contain a chalky fluid. They may grow rapidly or very slowly, and are found in children and adults. Both sexes are affected and there is no obvious tribal or geographical localization.

摘要

肯尼亚报告了26例肿瘤性钙化症病例。这种疾病常被误诊,病因不明。它表现为钙化肿瘤,通常出现在臀部和臀部周围的肌肉及皮下组织中。肿瘤部分为实性,部分为多房性囊肿,内含白垩样液体。它们可能生长迅速或非常缓慢,在儿童和成人中均有发现。男女均可患病,且无明显的部落或地理分布局限。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21d0/1982282/b896848dd08b/brmedj02015-0044-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21d0/1982282/81000dce4c53/brmedj02015-0032-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21d0/1982282/87ea49c5ff0d/brmedj02015-0032-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21d0/1982282/cb42c13645c6/brmedj02015-0044-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21d0/1982282/b896848dd08b/brmedj02015-0044-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21d0/1982282/81000dce4c53/brmedj02015-0032-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21d0/1982282/87ea49c5ff0d/brmedj02015-0032-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21d0/1982282/cb42c13645c6/brmedj02015-0044-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21d0/1982282/b896848dd08b/brmedj02015-0044-b.jpg

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本文引用的文献

1
Calcifying collagenolysis (tumoural calcinosis).钙化性胶原溶解(肿瘤性钙化症)
Br J Radiol. 1966 Jul;39(463):526-32. doi: 10.1259/0007-1285-39-463-526.
2
Tumoural calcinosis.
Br J Radiol. 1966 Jul;39(463):518-25. doi: 10.1259/0007-1285-39-463-518.
示指固有伸肌腱的肿瘤性钙化:一例报告。
Clin Case Rep. 2023 Jun 28;11(7):e7541. doi: 10.1002/ccr3.7541. eCollection 2023 Jul.
4
Uremic tumoral calcinosis: A case report.尿毒症性肿瘤性钙化:一例报告。
Arch Rheumatol. 2021 Feb 8;36(3):470-472. doi: 10.46497/ArchRheumatol.2021.8617. eCollection 2021 Sep.
5
Juxta-articular tumoral calcinosis associated with the temporomandibular joint: a case report and concise review.关节旁肿瘤性钙化与颞下颌关节相关:病例报告及简短综述。
BMC Oral Health. 2019 Jul 9;19(1):138. doi: 10.1186/s12903-019-0816-3.
6
Dialysis as a Treatment Option for a Patient With Normal Kidney Function and Familial Tumoral Calcinosis Due to a Compound Heterozygous FGF23 Mutation.透析作为一种治疗选择,用于治疗一位肾功能正常且存在家族性肿瘤性钙质沉着症的患者,该患者的病因是 FGF23 基因突变的复合杂合子。
Am J Kidney Dis. 2018 Sep;72(3):457-461. doi: 10.1053/j.ajkd.2017.12.020. Epub 2018 Mar 14.
7
A 23-year-old patient with secondary tumoral calcinosis: Regression after subtotal parathyroidectomy: A case report.一名23岁继发性肿瘤性钙化患者:甲状旁腺次全切除术后病情缓解:病例报告
Int J Surg Case Rep. 2016;23:56-60. doi: 10.1016/j.ijscr.2016.04.011. Epub 2016 Apr 11.
8
Review of tumoral calcinosis: A rare clinico-pathological entity.肿瘤性钙化综述:一种罕见的临床病理实体。
World J Clin Cases. 2014 Sep 16;2(9):409-14. doi: 10.12998/wjcc.v2.i9.409.
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Nephrol Dial Transplant. 2014 Dec;29(12):2155-7. doi: 10.1093/ndt/gfu270. Epub 2014 Aug 21.
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Familial tumoral calcinosis: from characterization of a rare phenotype to the pathogenesis of ectopic calcification.家族性肿瘤性钙化:从罕见表型的特征到异位钙化的发病机制。
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