Follicular immunoblastic lymphoma: a clinicopathologic and immunohistochemical study of a case

Xuanqiu He1, Lei Yang, Yanqing Ding

  • 1First Clinical Medical College, Department of Pathology, Southern Medical University, Guangzhou 510515, China. lmsh815@163.com

Insights

Primary follicular immunoblastic lymphoma (FIBL) is a rare cancer. This case report details its features, diagnosis, and poorer prognosis compared to follicular lymphoma.

Area of Science:

  • Hematology
  • Oncology
  • Pathology

Background:

  • Primary follicular immunoblastic lymphoma (FIBL) is an exceedingly rare type of lymphoma.
  • Understanding its clinicopathologic and immunohistochemical features is crucial for accurate diagnosis and management.

Observation:

  • This report details a rare case of FIBL in a Chinese female patient.
  • PET-CT imaging was utilized to assess systemic lymph node metastasis.
  • Differential diagnosis from follicular lymphoma (FL) and reactive follicular hyperplasia (RFH) was discussed.

Findings:

  • FIBL is characterized by a neoplastic proliferation of intrafollicular immunoblasts.
  • Positive CD10 expression suggests a germinal center origin, while CD138 positivity indicates plasmablastic differentiation.
  • FIBL exhibits a higher propensity for transformation into diffuse large B-cell lymphoma.

Implications:

  • Accurate identification of FIBL is essential for appropriate patient management.
  • Recognizing FIBL's potential for transformation impacts prognostic assessment.
  • This case contributes to the understanding of a rare lymphoma variant.

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