Cutaneous arteritis with compartment syndrome: Case report and review of published works

نویسندگان

چکیده

Abstract Cutaneous arteritis (CA) is a rare limited form of polyarteritis nodosa (PAN), which usually has benign prognosis and requires less aggressive therapy. Here, we present case CA localized to both skin muscle the same area as lesions. We propose with disorders severe subtype literature review disorders, may require treatment intravenous pulse methylprednisolone, immunosuppressive therapy, below‐the‐knee amputation. Our presented here demonstrates associated compartment syndrome, leading highly elevated serum concentration procalcitonin.

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Increased CA 125 in a patient with tuberculous peritonitis: case report and review of published works.

A case of a middle aged woman with weight loss, ascites, and a pleural effusion is presented where a clinical diagnosis of ovarian cancer was made. Her CA 125 was greatly increased at 873 IU/ml and the ascites was a lymphocytic exudate but cytology failed to show malignant cells. Operative biopsy showed numerous noncaseating granulomas in the omentum but no mycobacterial organisms were seen. Em...

متن کامل

Abdominal Compartment Syndrome after Cesarean Section: A Case Report

Background: Abdominal compartment syndrome (ACS) after cesarean section (CS) is a rare event which is associated with an increased risk of morbidity and mortality. This complication may arise as a result of musculoskeletal trauma and fluid accumulation. The present report aimed to introduce a case of ACS after the cesarean section. Case report: We present...

متن کامل

Adult rhabdomyosarcoma of the gall bladder: case report and review of published works.

A 90 year old woman with alveolar rhabdomyosarcoma of the gall bladder is described. The patient died with tumour metastasis four months after diagnosis despite complete excision of the tumour. The histological, immunohistochemical, and ultrastructural features of the tumour are summarised and published works are reviewed.

متن کامل

Cutaneous Manifestations in POEMS Syndrome: Case Report and Review

The authors report a case of sensorimotor polyneuropathy, diffuse cutaneous hyperpigmentation, skin sclerodermiform thickening and papular lesions in the infraclavicular and abdominal region. Besides weight loss, there were diabetes mellitus and hypothyroidism. The alterations were consistent with POEMS (Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal gammopathy and Skin changes) syndr...

متن کامل

Rothmund-Thomson Syndrome with Malignant Fibrous Histiocytoma: Report of a Case and Review of Literature

Rothmund–Thomson syndrome is a rare autosomal recessive genodermatosis characterized by early onset of poikiloderma and several other cutaneous and organ involvements. We are going to report a 14-year-old girl who has been diagnosed with Rothmund– Thomson syndrome since she was 3 years old and has been suffering from pain and swelling of the right elbow and forearm for about 6 months. There are...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: Journal of cutaneous immunology and allergy

سال: 2021

ISSN: ['2574-4593']

DOI: https://doi.org/10.1002/cia2.12165