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小隐静脉异位骨化及慢性静脉功能不全伴匐行性网状青斑的脂膜炎性骨化

Heterotopic ossification of small saphenous vein and panniculitis ossificans of chronic venous insufficiency presenting with livedo racemosa.

作者信息

Lekich Chris, Parsi Kurosh

机构信息

Venus Centre Vein Clinic, Brisbane, Australia.

Department of Dermatology, St. Vincent's Hospital, Sydney, Australia University of New South Wales, Sydney, Australia

出版信息

Phlebology. 2014 Jul;29(6):401-6. doi: 10.1177/0268355513495829. Epub 2013 Jul 11.

Abstract

OBJECTIVES

Livedo racemosa is a reticulate eruption that presents with branched and partially blanchable incomplete rings. Livedo racemosa is distinct from livedo reticularis, a similar condition that presents with a diffuse and symmetrical blanchable eruption. In contrast to livedo reticularis which may be physiological, livedo racemosa is always associated with an underlying pathology. To our knowledge, this is the first report of panniculitis ossificans and heterotopic ossification of small saphenous vein (SSV) presenting with livedo racemosa.

METHODS

We present a 70-year-old male referred for investigation and management of progressive pigmentation and 'lipodermatosclerosis' of lower limbs. There was no history of deep venous thrombosis but an earlier ultrasound had detected a non-occlusive thrombus in the left SSV. Examination and investigations revealed the skin eruption to be livedo racemosa and the associated subcutaneous induration and nodularity to be due to panniculitis ossificans. Biopsy of the SSV demonstrated segmental heterotopic ossification. Duplex ultrasound demonstrated bilateral superficial and deep venous incompetence but no evidence of an acute or chronic venous thrombosis. The patient was diagnosed with heterotopic ossification secondary to venous insufficiency and managed conservatively.

CONCLUSION

Livedo racemosa may be an early sign of panniculitis ossificans and its presence should trigger further diagnostic investigations.

摘要

目的

匐行性血管瘤是一种网状皮疹,表现为分支状且部分可褪色的不完全环状。匐行性血管瘤与网状青斑不同,网状青斑是一种类似情况,表现为弥漫性、对称性且可褪色的皮疹。与可能为生理性的网状青斑不同,匐行性血管瘤总是与潜在病理状况相关。据我们所知,这是首例以匐行性血管瘤表现的骨化性脂膜炎和小隐静脉(SSV)异位骨化的报告。

方法

我们报告一名70岁男性,因下肢进行性色素沉着和“脂膜皮肤硬化症”前来接受检查和治疗。患者无深静脉血栓形成病史,但早期超声检查发现左SSV有非闭塞性血栓。检查和调查显示皮肤皮疹为匐行性血管瘤,相关的皮下硬结和结节是由骨化性脂膜炎引起的。SSV活检显示节段性异位骨化。双功超声显示双侧浅静脉和深静脉功能不全,但无急性或慢性静脉血栓形成的证据。该患者被诊断为静脉功能不全继发异位骨化,并接受了保守治疗。

结论

匐行性血管瘤可能是骨化性脂膜炎的早期征象,其出现应引发进一步的诊断性检查。

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