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Deepali Gupta Surjit Singh Deepti Suri Jasmina Ahluwalia Reena Das Neelam Varma 《Rheumatology international》2010,30(6):767-770
The objectives of this study are to highlight the arthritic presentation of acute lymphoblastic leukemia (ALL) in children
and to delineate features that could help differentiate it from juvenile idiopathic arthritis (JIA). We present a retrospective
case control study based on records of the Pediatric Rheumatology Clinic, Advanced Pediatric Centre, Post Graduate Institute
of Medical Education and Research, Chandigarh, India for the period January 2005–October 2008. We compared the clinical profile
of 11 children referred to us with musculoskeletal complaints who were ultimately diagnosed to have ALL, with the clinical
profile of an equal number of age and sex matched children with JIA. Important features that predicted a diagnosis of ALL
and differentiated it from JIA were history of night pain (P = 0.001), non-articular bony pain (P = 0.001), presence of joint pain out of proportion to physical findings (P = 0.0001), anemia (P = 0.004), leucopenia (P = 0.045), lymphocytic predominance (P = 0.002) and thrombocytopenia (P = 0.012). In conclusion, children with musculoskeletal complaints are often referred to the rheumatologist for evaluation.
The treating physician should always exclude the possibility of an underlying ALL especially if there are atypical clinical
features or subtle hematological abnormalities. 相似文献
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Sidhu R McAlindon ME Kapur K Sanders DS 《Gastroenterology》2007,133(2):729; author reply 729-729; author reply 730
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Yong Kyong Kwon Reena C Jha Kambiz Etesami Thomas M Fishbein Metin Ozdemirli Chirag S Desai 《World journal of hepatology》2015,7(26):2696-2702
Reactive lymphoid hyperplasia(RLH), also known as pseudolymphoma or nodular lymphoid lesion of the liver is an extremely rare condition, and only 51 hepatic RLH cases have been described in the literature since the first case was described in 1981. The majority of these cases were asymptomatic and incidentally found through radiological imaging. The precise etiology of hepatic RLH is still unknown, but relative high prevalence of autoimmune disorder in these cases suggests an immune-based liver disorder. Imaging features of hepatic RLH often suggest malignant lesions such as hepatocellular carcinoma and cholangiocarcinoma. In this report, we discuss two cases of hepatic RLH in patients with autoimmune hepatitis. We also present pathologic and magnetic resonance imaging findings, including one case utilizing a hepatocellular contrast agent, Eovist. Definitive diagnosis of hepatic RLH often requires surgical excision. 相似文献
100.
Maheshkumar N Upasani Supriya Chopra Reena Engineer Umesh Mahantshetty Seema Medhi Zubin Mehta Shyam K Shrivastava 《The British journal of radiology》2015,88(1054)