Barking up the wrong tree: Vascular tree-in-bud due to intravascular lymphoma

IF 0.8 Q4 RESPIRATORY SYSTEM Respiratory Medicine Case Reports Pub Date : 2024-01-01 DOI:10.1016/j.rmcr.2024.102020
Ravi Manglani , Ji-Hae Shin , Venkata Sireesha Chemarthi , Mohamad Raji , Anna Rozenshtein , Oleg Epelbaum
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Abstract

A 59-year-old previously healthy woman presented with a six-month history of fever, nonproductive cough, and weight loss. The cause of these symptoms remained obscure despite a thorough, month-long hospitalization. On presentation, she was normotensive with a pulse of 98 beats/minute, respiratory rate of 20 breaths/minute, and a temperature of 39.4C. She was emaciated. Physical examination was notable for faint bibasilar crackles on lung auscultation. Initial laboratory testing revealed pancytopenia. Peripheral smear demonstrated normocytic, normochromic anemia without immature cells or schistocytes. Other notable laboratory findings included elevated levels of lactate dehydrogenase, elevated ferritin, and elevated levels of fasting serum triglycerides. A comprehensive laboratory evaluation for connective tissue disease was negative. Plain chest radiography was normal while computed tomography (CT) of the chest demonstrated sub-centimeter nodules in a branching centrilobular pattern as well as in a peri-lymphatic distribution without associated lymphadenopathy or organomegaly.

The above constellation of laboratory abnormalities raised concern for hemophagocytic lymphohistiocytosis (HLH). Soluble IL-2 (CD25) receptor levels were markedly elevated. Bronchoscopy with transbronchial biopsies of the right lower lobe was performed, revealing intravascular lymphoma associated with HLH. Our case emphasizes the need for clinicians to consider vascular causes of tree - in-bud nodules in addition to the conventional bronchiolar causes. The case also is a reminder of the need to conduct an exhaustive search for malignancy, in patients with HLH.

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误入歧途血管内淋巴瘤引起的血管树瘤
一名 59 岁的健康妇女因发烧、无排气性咳嗽和体重减轻前来就诊,病史长达 6 个月。尽管经过长达一个月的彻底住院治疗,但这些症状的病因仍然不明。就诊时,她的血压正常,脉搏 98 次/分,呼吸频率 20 次/分,体温 39.4 摄氏度。她面容憔悴。体格检查时,肺部听诊有微弱的双肺裂音。初步实验室检查显示她患有全血细胞减少症。外周血涂片显示为正常红细胞、正常色素性贫血,无未成熟细胞或血吸虫。其他值得注意的实验室检查结果包括乳酸脱氢酶水平升高、铁蛋白升高和空腹血清甘油三酯水平升高。结缔组织病的综合实验室评估结果为阴性。胸部X线平片检查正常,胸部计算机断层扫描(CT)显示,该患者的胸腔内有一厘米以下的结节,呈树枝状分布,淋巴周围也有分布,但没有伴有淋巴结肿大或器官肿大。可溶性IL-2(CD25)受体水平明显升高。对患者的右下叶进行了支气管镜检查和经支气管活检,发现血管内淋巴瘤与HLH有关。我们的病例强调,除了传统的支气管病因外,临床医生还需要考虑树-芽内结节的血管病因。该病例还提醒我们,对于 HLH 患者,需要进行详尽的恶性肿瘤筛查。
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来源期刊
Respiratory Medicine Case Reports
Respiratory Medicine Case Reports RESPIRATORY SYSTEM-
CiteScore
2.10
自引率
0.00%
发文量
213
审稿时长
87 days
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