一例罕见的淋巴结外边缘区淋巴瘤模拟腹部茧综合征的青少年患者。

IF 1.3 4区 医学 Q3 PATHOLOGY Pediatric and Developmental Pathology Pub Date : 2024-01-01 Epub Date: 2023-10-30 DOI:10.1177/10935266231205511
Timothy J D Ohlsen, Ryan J Morse, Hira Ahmad, Maria Cristina Pacheco, Katherine E Debiec, Sandra D Bohling
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引用次数: 0

摘要

黏膜相关淋巴组织的淋巴结外边缘区淋巴瘤(MALT淋巴瘤)是一种在儿科患者中罕见的惰性非霍奇金淋巴瘤。MALT淋巴瘤最常见于胃肠道或眶周组织,可能是慢性抗原刺激或免疫失调的后遗症。罕见的MALT淋巴瘤发生于妇科,在老年患者中有报道。我们报告了一名16岁青春期后女性的独特病例,该女性患有局限于妇科的MALT淋巴瘤,最初表现为腹部胀满、异常子宫出血和继发于尿流梗阻的梗阻性急性肾损伤。术中发现子宫和左输卵管致密性纤维化,类似于腹茧综合征。她接受了6个周期的bendamustine和利妥昔单抗治疗,解剖和代谢完全缓解。在本报告中,我们强调了儿科人群中罕见恶性肿瘤的一种非常不寻常的表现,以及考虑到该患者的年轻年龄和肿瘤位置的独特治疗考虑因素。
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An Unusual Case of Extranodal Marginal Zone Lymphoma Mimicking Abdominal Cocoon Syndrome in an Adolescent Patient.

Extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue (MALT lymphoma) is an indolent non-Hodgkin lymphoma rarely seen in pediatric patients. MALT lymphoma most commonly involves the gastrointestinal tract or peri-orbital tissues, potentially as sequela of chronic antigenic stimulation or immune dysregulation. Rare cases of MALT lymphoma arising from the gynecologic tract have been reported in older adult patients. We present the unique case of a 16-year-old postpubescent female with MALT lymphoma localized to the gynecologic tract, who initially presented with abdominal fullness, abnormal uterine bleeding, and obstructive acute kidney injury secondary to urinary outflow obstruction. Intraoperatively, dense fibrosis of the uterus and left fallopian tube was noted which mimicked abdominal cocoon syndrome. She was treated with 6 cycles of bendamustine and rituximab with complete anatomic and metabolic remission. In this report we highlight a very unusual presentation of a rare malignancy in the pediatric population as well as unique treatment considerations given this patient's young age and tumor location.

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来源期刊
CiteScore
3.70
自引率
5.30%
发文量
59
审稿时长
6-12 weeks
期刊介绍: The Journal covers the spectrum of disorders of early development (including embryology, placentology, and teratology), gestational and perinatal diseases, and all diseases of childhood. Studies may be in any field of experimental, anatomic, or clinical pathology, including molecular pathology. Case reports are published only if they provide new insights into disease mechanisms or new information.
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