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原发性脾淋巴瘤:当前的诊断趋势

Primary splenic lymphoma: Current diagnostic trends.

作者信息

Ingle Sachin B, Hinge Ingle Chitra R

机构信息

Sachin B Ingle, Department of Pathology, MIMSR Medical College, Latur, Maharashtra 4132512, India.

出版信息

World J Clin Cases. 2016 Dec 16;4(12):385-389. doi: 10.12998/wjcc.v4.i12.385.

Abstract

The primary splenic lymphoma is extremely uncommon, can present with grave complications like hypersplenism and splenic rupture. In view of vague clinical presentation, it is difficult to arrive at the diagnosis. In such circumstances, histopathological diagnosis is very important. A precise diagnosis can only be made on histopathology and confirmed on immunohistochemistry.Emergency splenectomy is preferred as an effective therapeutic and diagnostic tool in cases with giant splenomegaly. Core biopsy is usually not advised due to a high risk of post-core biopsy complications in view of its high vascularity and fragility. Aim behind highlighting the topic is to specify that core biopsy/ fine needle aspiration cytology can be used as an effective diagnostic tool to arrive at correct diagnosis to prevent untoward complications related to disease and treatment. Anticoagulation therapy is vital after splenectomy to avoid portal splenic vein thrombosis.

摘要

原发性脾淋巴瘤极为罕见,可出现脾功能亢进和脾破裂等严重并发症。鉴于临床表现模糊,很难做出诊断。在这种情况下,组织病理学诊断非常重要。只有通过组织病理学才能做出准确诊断,并通过免疫组织化学加以证实。对于巨脾病例,急诊脾切除术作为一种有效的治疗和诊断手段更为可取。鉴于脾脏血管丰富且脆弱,穿刺活检后并发症风险高,通常不建议进行穿刺活检。强调该主题的目的是明确穿刺活检/细针穿刺细胞学检查可作为一种有效的诊断工具,以做出正确诊断,预防与疾病和治疗相关的不良并发症。脾切除术后抗凝治疗对于避免门静脉脾静脉血栓形成至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cd3/5156875/e083c2f65614/WJCC-4-385-g001.jpg

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