Concurrent Langerhans cell histiocytosis and acute myeloid leukemia: A rare presentation of a rare case.
Julia L GaoMatthew J DavisAlicia T DagrosaShabnam MomtahenPublished in: Journal of cutaneous pathology (2023)
A 72-year-old woman with no significant past medical history was admitted to the hospital for new-onset of leukocytosis with neutropenia, anemia, and thrombocytopenia, as well as a pruritic skin eruption. She was found to have acute myeloid leukemia (AML) with myelomonocytic differentiation. Her skin eruption consisted of widespread hemorrhagic crusted papules on the scalp and trunk. A skin biopsy was performed, which revealed a proliferation of mononuclear cells in the dermis with prominent epidermotropism and positive expression of CD1a and langerin (CD207), supporting a diagnosis of Langerhans cell histiocytosis (LCH). LCH is an uncommon proliferative disorder of activated Langerhans cells, which generally presents in children. In adults, it is exceptionally infrequent. Associated malignancies and rare reports of AML developing in subsequent years after an initial presentation of LCH have been described. Here we present an unusual concurrent presentation of LCH and AML in an adult.
Keyphrases
- acute myeloid leukemia
- induced apoptosis
- allogeneic hematopoietic stem cell transplantation
- single cell
- rare case
- cell cycle arrest
- soft tissue
- healthcare
- wound healing
- signaling pathway
- case report
- poor prognosis
- young adults
- endoplasmic reticulum stress
- stem cells
- chronic kidney disease
- squamous cell carcinoma
- cell death
- acute lymphoblastic leukemia
- bone marrow
- pi k akt
- binding protein
- radiation therapy
- long non coding rna
- cell proliferation
- fine needle aspiration