非霍奇金淋巴瘤的视图来源

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您请求的操作仅限于组中的用户:==特征/临床表现==[[文件:淋巴瘤淋巴结图。jpg|367x367px|右|无边框]]*患者表现为发热、体重减轻或盗汗，也称为B型症状。*系统性B症状在非霍奇金淋巴瘤的高级别变异型患者中更为常见。*超过三分之二的患者表现为无痛性周围淋巴结病。*低级别淋巴瘤可出现淋巴结病变的盛衰发作，并伴有其他症状。*淋巴结肿大*苍白*疲劳*出血*感染*皮肤发红来源不明的全身瘙痒*不明原因的胸部、腹部或骨骼疼痛美国国家癌症研究所。成人非霍奇金淋巴瘤治疗。2009-09-10;2010 - 02。可从:(http://www.cancer.gov/cancertopics/pdq/treatment/adult-non-hodgkins/Patient)患者有不同的表现，并根据所涉及的部位而变化。*伯基特淋巴瘤:患者通常有快速增长的肿瘤肿块。 This type of lymphoma may present with tumor lysis syndrome. * Endemic (African) form may have a jaw or facial bone tumors in 50 to 60 percent of cases. The primary involvement of the abdomen is less common. The primary tumor can spread to extranodal sites like mesentery, ovary, testis, kidney, breast, and meninges. * About 50 percent of patients may develop the extranodal disease (secondary extranodal disease), while between 10 and 35 percent of patients will have primary extranodal lymphoma at the time of diagnosis. Extranodal sites of involvement may include the nasopharynx, GI tract, bone, thyroid, testes and soft tissue. Abdominal lymphoma may cause abdominal pain & fullness, GI obstruction or bleeding, ascites, back pain & leg swelling. Lymph node enlargement in the chest can lead to compression of the trachea or bronchus, causing shortness of breath & coughing.Goodman C.C., Fuller, K.S. Pathology: Implications for the Physical Therapist. 3rd Ed. Missouri, Saunders; Elsevier; 2009. * Primary CNS lymphoma is a NHL restricted to the nervous system. Presenting symptoms may include: headache, confusion, seizures, extremity weakness/numbness, personality changes, difficulty speaking & lethargy. (Prior to the spread of HIV, this type of lymphoma was rare.)

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