dystrophic calcinosis cutis and sle; the bone scan pattern [persian]
Authors
abstract
a 21 years old woman presented with a history of sle and skin lesions on the arms, trunk, and abdomen. the left gluteal region was ulcerated and painful and occasionally extruded a chalky white material. the patient referred from rheumatology department for osteomyelitis assessment. on physical examination the patient had hard, nontender lesions on the proximal arms, lower abdomen and lower back. she had painful, hyper pigmented bullae, plaques, erosions and ulcer on her hands, arms, thighs, knees and especially left gluteal region. all laboratory results including bun, cr, ca, ph, lft, were normal except for esr which was increased. left gluteal skin biopsy reveals homogenized and sclerotic collagen in the lower dermis with scattered foci of calcification, consistent with calcinosis cutis. the whole body bone scan shows diffuse extra osseous calcification mainly in the arms, lower trunk and thighs. the x-ray findings revealed multiple foci of calcification in the soft tissue compartment of the arms and lower trunk. focal areas of increased uptake in the ribs and right humerus secondary to osteoporosis and truma were noticed. calcinosis cutis is a rare presentation of sle. it is usually seen in crf and due to electrolyte impairment .in this report however, a case of sle is presented with extensive calcinosis but normal renal function and lack of any electrolyte imbalance.
similar resources
Dystrophic calcinosis cutis and SLE; the bone scan pattern [Persian]
A 21 years old woman presented with a history of SLE and skin lesions on the arms, trunk, and abdomen. The left gluteal region was ulcerated and painful and occasionally extruded a chalky white material. The patient referred from rheumatology department for osteomyelitis assessment. On physical examination the patient had hard, nontender lesions on the proximal arms, lower abdomen and low...
full text[Facial dystrophic calcinosis cutis secondary to acne].
Actas Dermosifiliogr. 2009;100:615-34 622 squamous cell carcinoma5,6; the incidence is higher in men with long-standing lesions situated on the head, neck, or other areas exposed to sunlight.7 The molecular mechanism of this transformation is not fully understood. A number of theories implicate the proteins involved in regulation of the cell cycle, alterations of which could lead to the appeara...
full textDiscoid lupus erythematosus with dystrophic calcinosis cutis
CC: calcinosis cutis DLE: discoid lupus erythematosus SLE: systemic lupus erythematosus INTRODUCTION Calcinosis cutis (CC) is a rare disorder known to occur commonly in association with underlying autoimmune connective tissue diseases. CC primarily occurs in patients with dermatomyositis, systemic scleroderma, and mixed connective tissue disease. It is only rarely associated with systemic lupus...
full textCalcinosis cutis.
1 of 2 DESCRIPTION An 87-year-old woman with a history of hypertension, atrial fi brillation, and mixed connective tissue disease was admitted to hospital because of heart failure. Besides clinical signs of ventricular dysfunction, physical examination showed painless, subcutaneous nodules that had developed during the past 10 years on her left elbow ( fi gure 1A ) and knees ( fi gure 1B , righ...
full textCalcinosis Cutis and Calciphylaxis.
Calcinosis cutis (CC) is defined as the deposition of calcium salts in the skin. The condition is divided into 5 types: calciphylaxis and dystrophic, metastatic, idiopathic, and iatrogenic CC. Dystrophic CC is the most common form and usually occurs in association with autoimmune diseases. CC can be treated surgically or with the use of drugs such as diltiazem, bisphosphonates, warfarin, ceftri...
full textMy Resources
Save resource for easier access later
Journal title:
iranian journal of nuclear medicinePublisher: tehran university of medical sciences
ISSN 1681-2824
volume 12
issue 2 2004
Hosted on Doprax cloud platform doprax.com
copyright © 2015-2023