Rai Namrita, Azhar Zeenat Amna, Kheli Neelum Tahir, Lateef Fozia, Javed Omer, Raza Muhammad Rafie
Department of Pediatric Hematology and Oncology, Indus Hospital & Health Network, Karachi 75190, Pakistan.
https://orcid.org/0000-0002-6300-8961.
Ecancermedicalscience. 2024 May 10;18:1702. doi: 10.3332/ecancer.2024.1702. eCollection 2024.
Discordant lymphoma (DL) is an uncommon condition in which two or more histologically different types of lymphomas are present at distinct anatomical sites in the same patient. Here, we report a case of a pediatric patient under 10 years old presenting with symptoms of general sickness with cervical lymphadenopathy, abdominal distension and an abdominal mass. Upon conducting investigations, classic Hodgkin lymphoma (CHL) was detected in the cervical lymph nodes, and high-grade B-cell non-Hodgkin lymphoma was detected in the bone marrow and abdominal mass. The patient was therefore diagnosed with DL. The boy was initially diagnosed with CHL but proceeded to have aggressive disease progression, due to which further workup was done. In the past, literature reports have been published for adult cases of DL, and currently, research is being conducted to formulate treatment protocols for it. However pediatric cases of DL remain widely undiscussed. Since we are dealing with a rare or widely underreported condition, we found it significant to elaborate on its clinical presentation, treatment plan, complications and prognosis.
异质性淋巴瘤(DL)是一种罕见的疾病,同一患者的不同解剖部位存在两种或更多种组织学不同类型的淋巴瘤。在此,我们报告一例10岁以下儿科患者,出现全身不适症状,伴有颈部淋巴结肿大、腹胀和腹部肿块。经检查,在颈部淋巴结中检测到经典型霍奇金淋巴瘤(CHL),在骨髓和腹部肿块中检测到高级别B细胞非霍奇金淋巴瘤。因此,该患者被诊断为DL。该男孩最初被诊断为CHL,但疾病进展迅速,因此进行了进一步检查。过去,已有成人DL病例的文献报道,目前正在开展研究以制定其治疗方案。然而,儿科DL病例仍未得到广泛讨论。由于我们处理的是一种罕见或报道不足的疾病,我们认为详细阐述其临床表现、治疗方案、并发症和预后具有重要意义。