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Related Concept Videos

  1. Home
  2. Research Domains
  3. Biomedical And Clinical Sciences
  4. Immunology
  5. Immunology Not Elsewhere Classified
  6. Resolution Of Erythema Nodosum Following Flt3-targeted Therapy In Acute Myeloid Leukemia: A Case Report.
  1. Home
  2. Research Domains
  3. Biomedical And Clinical Sciences
  4. Immunology
  5. Immunology Not Elsewhere Classified
  6. Resolution Of Erythema Nodosum Following Flt3-targeted Therapy In Acute Myeloid Leukemia: A Case Report.

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Resolution of Erythema Nodosum Following FLT3-Targeted Therapy in Acute Myeloid Leukemia: A Case Report.

Risa Nakane1, Romane Teshima1, Natsuko Saito-Sasaki1

  • 1Dermatology, University of Occupational and Environmental Health, Kitakyushu, JPN.

Cureus
|March 17, 2025

View abstract on PubMed

Summary
This summary is machine-generated.

Erythema nodosum (EN) in a patient with acute myeloid leukemia (AML) was linked to a FLT3 mutation, a common driver in AML-M2. This highlights FLT3

Keywords:
case reporterythema nodosumflt3-itd mutationleukemia

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Area of Science:

  • Hematology
  • Dermatology
  • Oncology

Background:

  • Acute myeloid leukemia (AML) can present with paraneoplastic dermatological manifestations.
  • Erythema nodosum (EN) is an inflammatory condition characterized by tender subcutaneous nodules, typically on the lower legs.
  • FLT3 mutations are frequently observed in AML subtypes M2 and M4.

Observation:

  • A 59-year-old woman presented with persistent lower-leg erythema and pain, initially misdiagnosed as cellulitis.
  • The patient was diagnosed with EN and acute myeloid leukemia (AML), FAB subtype M2, harboring a FLT3-internal tandem duplication (ITD) mutation.

Findings:

  • FLT3-ITD mutations activate signaling pathways (PI3K/AKT, STAT5) that promote the production of pro-inflammatory cytokines.
  • These cytokines, including TNF-α, IL-1β, IL-6, and GM-CSF, contribute to the development of EN as a paraneoplastic phenomenon in AML.
paraneoplastic syndrome
  • The case demonstrates a direct link between FLT3 mutations in AML and inflammatory processes like EN.
  • Implications:

    • Distinguishing paraneoplastic EN from drug-induced EN is crucial for appropriate AML treatment strategies.
    • Understanding the role of FLT3 mutations in AML-associated inflammation can lead to targeted therapies.
    • This case underscores the importance of a multidisciplinary approach in diagnosing and managing complex hematologic and dermatologic conditions.