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伴宫颈癌的副肿瘤性皮肌炎:一种罕见的临床关联。

Paraneoplastic dermatomyositis with carcinoma cervix: a rare clinical association.

作者信息

Kumar Sumir, Mahajan B B, Kaur Sandeep, Singh Amarbir

机构信息

GGS Medical College & Hospital, Sadiq Road, Faridkot, Punjab 151203, India.

GGS Medical College & Hospital, Sadiq Road, Faridkot, Punjab 151203, India ; Skin OPD, GGS Medical College & Hospital, OPD Block, 1st Floor, Sadiq Road, Faridkot, Punjab 151203, India.

出版信息

Case Rep Dermatol Med. 2014;2014:836246. doi: 10.1155/2014/836246. Epub 2014 Dec 18.

DOI:10.1155/2014/836246
PMID:25587465
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4281437/
Abstract

Dermatomyositis is an uncommon inflammatory myopathy associated with cutaneous manifestations. It may also occur as paraneoplastic syndrome associated with various malignancies, most common of which being lung, breast, stomach, rectum, kidney, or testicular cancer. A postmenopausal woman presented to us with generalized itching along with skin rash and proximal muscle weakness of 2 years' duration. Examination revealed heliotrope rash and mechanic hands and muscle power 2/5 in proximal muscle groups of both upper and lower limbs. A clinical diagnosis of dermatomyositis was made which was supported by raised lactate dehydrogenase levels and skin biopsy findings. Past history was significant for vaginal discharge and bleeding per vagina. Further work-up revealed carcinoma cervix and she was referred to oncology department for further management. Temporal relationship and improvement of muscle weakness with treatment of underlying neoplasm supported its paraneoplastic nature. So, final diagnosis of keratinizing squamous cell carcinoma of cervix with paraneoplastic dermatomyositis was made. A nationwide cohort study of 1,012 patients with dermatomyositis in Taiwan revealed only 3 patients with cervical cancer. So this case is being reported for its rare association with carcinoma cervix and to highlight the need of detailed evaluation for underlying malignancies in patients with dermatomyositis.

摘要

皮肌炎是一种罕见的炎性肌病,伴有皮肤表现。它也可能作为副肿瘤综合征与各种恶性肿瘤相关,其中最常见的是肺癌、乳腺癌、胃癌、直肠癌、肾癌或睾丸癌。一位绝经后女性前来就诊,有全身瘙痒、皮疹以及持续2年的近端肌无力症状。检查发现有向阳疹、技工手,上下肢近端肌群肌力为2/5。临床诊断为皮肌炎,乳酸脱氢酶水平升高及皮肤活检结果支持这一诊断。既往史有阴道分泌物及阴道出血。进一步检查发现宫颈癌,她被转诊至肿瘤科进一步治疗。肌无力与潜在肿瘤治疗之间的时间关系及改善情况支持其副肿瘤性质。因此,最终诊断为宫颈角化性鳞状细胞癌伴副肿瘤性皮肌炎。台湾一项对1012例皮肌炎患者的全国性队列研究显示,仅有3例患有宫颈癌。因此,报道此病例是因其与宫颈癌的罕见关联,并强调对皮肌炎患者进行潜在恶性肿瘤详细评估的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed48/4281437/8ece850e6192/CRIDM2014-836246.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed48/4281437/87046781bdef/CRIDM2014-836246.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed48/4281437/8ece850e6192/CRIDM2014-836246.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed48/4281437/87046781bdef/CRIDM2014-836246.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed48/4281437/8ece850e6192/CRIDM2014-836246.002.jpg

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