B-Acute Lymphoblastic Leukemia/Lymphoblastic Lymphoma Mimicking Fibrosing Mediastinitis: A Case Report and Diagnostic Insight.

IF 1 Q3 MEDICINE, GENERAL & INTERNAL American Journal of Case Reports Pub Date : 2024-12-30 DOI:10.12659/AJCR.945804
Aya Kitamura, Shigehisa Yanagi, Kotaro Shide, Yuichiro Sato, Ayako Kamiunten, Yasuhiro Yamanari, Akiko Kitamura, Makoto Sumiyoshi, Yasuharu Oda, Hironobu Tsubouchi, Kazuya Shimoda, Taiga Miyazaki
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Abstract

BACKGROUND Fibrosing mediastinitis (FM) is a rare, fibroproliferative disorder within the mediastinum. It is extremely rare for hematologic malignancies to develop as FM. CASE REPORT A 32-year-old Japanese man with a 1-month history of headache and 2-week history of facial swelling underwent chest computed tomography (CT); a diffuse mass-like lesion was revealed in the anterior mediastinum with severe stenosis of vital mediastinal organs. After a surgical biopsy, an initial diagnosis of idiopathic FM was made. The FM lesions responded mildly to corticosteroids but recurred repeatedly. Sixteen months after the treatment initiation, blasts appeared in the peripheral blood (PB), and the patient was diagnosed with B-acute lymphoblastic leukemia/lymphoblastic lymphoma (B-ALL/LBL). Chemotherapy led to complete remission of the B-ALL/LBL and almost complete disappearance of FM-like lesions. Immunohistochemistry of the mediastinal biopsy specimen taken before the blasts' appearance in PB demonstrated a CD34/CD7/terminal deoxynucleotidyl transferase-positive population, an identical pattern of expression common to the blasts in the patient's PB and bone marrow. CONCLUSIONS This is the first case report of B-ALL/LBL presenting as FM. This case underscores the importance of considering the possibility of latent hematologic malignancy even in the absence of new symptoms other than those caused by FM lesions for a long period of time. This is the first demonstration that leukemia cells may be present in the FM lesions from the initial stage of disease onset. Even if a diagnosis of idiopathic FM is confirmed, continued suspicion of the presence of hematologic malignancy is vital for improving patient outcomes.

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急性b淋巴母细胞白血病/淋巴母细胞淋巴瘤模拟纤维化纵隔炎:1例报告和诊断见解。
背景:纤维化性纵隔炎(FM)是一种罕见的纵隔纤维增生性疾病。恶性血液病发展为FM是极为罕见的。病例报告一名32岁的日本男性,头痛1个月,面部肿胀2周,接受胸部计算机断层扫描(CT);前纵隔可见弥漫性肿块样病变,主要纵隔脏器严重狭窄。手术活检后,初步诊断为特发性FM。皮质类固醇对FM病变反应轻微,但反复复发。开始治疗16个月后,外周血中出现母细胞(PB),患者被诊断为b急性淋巴细胞白血病/淋巴细胞淋巴瘤(B-ALL/LBL)。化疗导致B-ALL/LBL完全缓解,fm样病变几乎完全消失。在PB中出现原细胞之前,纵隔活检标本的免疫组织化学显示CD34/CD7/末端脱氧核苷酸转移酶阳性群体,与患者PB和骨髓中原细胞的表达模式相同。结论:这是第一例以FM表现的B-ALL/LBL。本病例强调了考虑潜在血液恶性肿瘤可能性的重要性,即使在没有新症状的情况下,除了长期由FM病变引起的症状。这是首次证明白血病细胞可能存在于FM病变从疾病发作的初始阶段。即使确诊为特发性FM,持续怀疑血液恶性肿瘤的存在对于改善患者预后至关重要。
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来源期刊
American Journal of Case Reports
American Journal of Case Reports Medicine-Medicine (all)
CiteScore
1.80
自引率
0.00%
发文量
599
期刊介绍: American Journal of Case Reports is an international, peer-reviewed scientific journal that publishes single and series case reports in all medical fields. American Journal of Case Reports is issued on a continuous basis as a primary electronic journal. Print copies of a single article or a set of articles can be ordered on demand.
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