Granulomatous cutaneous T-cell lymphoma in a patient with atage IVB of mycosis fungoides: a case report and literature review - Report - MDSpire

Granulomatous cutaneous T-cell lymphoma in a patient with atage IVB of mycosis fungoides: a case report and literature review

  • By

  • Zhu Lin

  • Jing Xue

  • Guozeng Ye

  • Shuang Li

  • Tingzhi Liu

  • Jiping Lang

  • Zhixin Zheng

  • Xiaoyan Li

  • Qinbo Wang

  • Junrong Chen

  • June 10, 2026

  • 0 min

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Clinical Report: Granulomatous Mycosis Fungoides in a Stage IVB Patient

Overview

This report presents a case of granulomatous mycosis fungoides (GMF) in a 57-year-old male, highlighting the clinical and histological features that distinguish GMF from other inflammatory skin disorders. The findings underscore the importance of accurate diagnosis and awareness of GMF's unique characteristics among healthcare professionals.

Background

Granulomatous mycosis fungoides (GMF) is a rare variant of mycosis fungoides, which is the most common form of primary cutaneous T-cell lymphoma. Accurate diagnosis is critical as GMF can mimic other inflammatory skin conditions, leading to potential misdiagnosis and inappropriate treatment. Understanding GMF's clinical and histological features is essential for effective management and improved patient outcomes.

Data Highlights

No numerical data or trial data presented in the article.

Key Findings

  • The patient was initially misdiagnosed with psoriasis, highlighting the diagnostic challenges of GMF.
  • Histological evaluation revealed tumor cell characteristics including positivity for CD3+ and negativity for CD7−, CD4−, and CD8−.
  • Immunohistochemical evaluations showed diffuse positivity for T-cell lineage markers (CD2 and CD3).
  • Absence of CD56 indicated active hyperplastic states within the bone marrow.
  • TCRβ and γ gene detection confirmed the presence of a clonal process.
  • GMF can be confused with other granulomatous diseases, necessitating careful histological examination.

Clinical Implications

Clinicians should maintain a high index of suspicion for granulomatous mycosis fungoides in patients presenting with atypical skin lesions, particularly those previously diagnosed with inflammatory skin disorders. Accurate diagnosis through histological evaluation is crucial for appropriate management and treatment planning.

Conclusion

Granulomatous mycosis fungoides is a distinct variant of mycosis fungoides that requires careful clinical and histological assessment to avoid misdiagnosis. Increased awareness among healthcare professionals can lead to better patient outcomes through timely and appropriate treatment.

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