نتایج جستجو برای: leukemia cutis
تعداد نتایج: 285906 فیلتر نتایج به سال:
Primary cutaneous involvement in T-cell acute lymphoblastic leukemia (ALL) is rare in elderly patients. Here we present a case of 65 years old male admitted to a metropolitan tertiary care hospital because of maculo-papular lesions on chest and back for last 3 months as chief complaint along with on and off history of fever, fatigability and anorexia. On general examination, there was no lympha...
Cutis laxa is a heterogeneous condition characterized by redundant, sagging, inelastic, and wrinkled skin. The inherited forms of this disease are rare and can have autosomal dominant, autosomal recessive, or X-linked inheritance. Three of the autosomal recessive cutis laxa syndromes, namely cutis laxa IIA (ARCL2A), cutis laxa IIB (ARCL2B), and geroderma osteodysplastica (GO), have very similar...
CMAJ • FEBRUARY 9, 2010 • 182(2) © 2010 Canadian Medical Association or its licensors 171 Apreviously healthy four-year-old girl presented with a rash of sudden onset consisting of erythematous macules on both cheeks (Figure 1) that were neither itchy nor tender and did not blanch. Over the next week, the rash spread from her cheeks to her arms, back, thighs and buttocks, and became papular and...
BACKGROUND Total skin electron irradiation (TSEI) is a special radiotherapy technique which has generally been used for treating adult patients with mycosis fungoides. Recently, two infants presented with leukemia cutis isolated to the skin requiring TSEI. This work discusses the commissioning and quality assurance (QA) methods for implementing a modified Stanford technique using a rotating har...
Iatrogenic calcinosis cutis presents with similar symptoms and signs of soft tissue, joint and bone infections. We present here a preterm infant with iatrogenic calcinosis cutis misdiagnosed as septhic arthritis and osteomyelitis. We hope that our case report helps to raise clinicians’awareness of this rare situation. .When swelling and erythema of extremities occur in a newborn infant after in...
A new-born male baby with typical features of Adams-Oliver syndrome (AOS) is described. Adams-Oliver syndrome is the association of aplasia cutis congenita with terminal transverse limb reduction defects with or without cutis marmorata telangiectatica congenita. The patient presented with brachydactyly involving all the digits of his hands and shortening of both big toes along with aplasia cuti...
cutis laxa (cl) is a rare congenital and acquired disorder characterized by loose and redundant skin with reduced elasticity. three types of congenital cutis laxa have been recognized. other findings are pulmonary emphysema, bronchiectasia, hernia and diverticulosis. we describe a female neonate involved by cutis laxa syndrome and a positive family history. we focus on the radiologic findings o...
We report a case of idiopathic calcinosis cutis diagnosed by fine needle aspiration cytology in a 50-yr-old female who presented with a subcutaneous swelling near the left iliac crest. Cytological finding of amorphous calcium salts with histiocytes and the appropriate clinical background led to the cytodiagnosis of idiopathic calcinosis cutis as subsequently confirmed on histopathology. Pitfall...
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