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CD30 Expression Is Rare in Myeloid Leukemia Cutis: A Study of 55 Cases and Implications for Routine Diagnostic
Olakunle Ogunrinade1, David Terrano, April Chiu
1*Department of Dermatology, Weill Cornell Medical College, New York, NY; and †Department of Pathology, Memorial Sloan-Kettering Cancer Center, New York, NY.
Insights
CD30 expression in skin infiltrates can indicate lymphoproliferative disorders. However, this study found CD30 positivity is rare in myeloid leukemia cutis, suggesting limited immunohistochemistry may suffice.
Area of Science:
- Dermatopathology
- Hematopathology
- Immunohistochemistry
Background:
- CD30 expression in cutaneous infiltrates typically suggests a CD30 lymphoproliferative disorder.
- Myeloid and other hematologic malignancies can also express CD30, complicating diagnosis.
- Leukemia cutis (LC) diagnosis requires careful consideration of CD30 expression patterns.
Purpose of the Study:
- To determine the prevalence of CD30 expression in leukemia cutis (LC).
- To assess if extensive immunohistochemical workup is necessary for all CD30-positive cutaneous infiltrates.
- To differentiate CD30-positive lymphoid versus myeloid malignancies in skin.
Main Methods:
- Retrospective analysis of 55 biopsies from 41 patients diagnosed with leukemia cutis.
- Evaluation of CD30 expression intensity and cellular distribution in blastoid infiltrates.
- Immunohistochemical staining for CD30, CD34, and CD117.
Main Results:
- CD30-positive mononuclear cells were found in 22 of 55 (40%) LC biopsies.
- Lymphocytic infiltrates showed strong CD30 staining (cytoplasmic/Golgi) in 18 biopsies.
- Myeloid leukemia cases rarely showed CD30 positivity, typically with weak (1+) staining.
Conclusions:
- CD30 positivity in myeloid leukemia cutis is uncommon and usually presents with weak staining.
- Strong, diffuse CD30 staining suggests a reactive lymphoid or lymphoproliferative process.
- In low clinical suspicion for CD30+ LC, extensive immunohistochemistry may be unnecessary.
Abstract:
Expression of CD30 in blastoid cutaneous infiltrates typically signifies a CD30 lymphoproliferative disorder, often requiring minimal immunohistochemical workup, if clinically consonant. However, myeloid and other hematologic malignancies often express CD30. We retrospectively examined the prevalence of CD30 expression in 41 patients (median age 59) and 55 biopsies with the diagnosis of leukemia cutis (LC) to determine whether an extensive immunohistochemical workup is warranted in all large, round cell CD30 cutaneous infiltrates. Each patient had refractory or recurrent disease, the histologic presence of a large mononuclear cell infiltrate, and varied cytogenetics. CD30 mononuclear cells within the infiltrate ranged from rare to many in 22 biopsies (22/55). In 18 biopsies, CD30 cells were interpreted as lymphocytic based on morphology, strong cytoplasmic and Golgi staining for CD30, and negative CD34 and CD117 staining. One case showing 3+ staining of lymphocytes was identified as a posttransplant lymphoproliferative disorder. The second 3+ case was favored to represent a subset of CD30-positive acute myeloid leukemia. Three other cases with 1+ membranous and cytoplasmic staining were interpreted as myeloid leukemia. In conclusion, CD30 positivity in myeloid leukemia in the skin is rare and does not often exhibit the strong membranous (2+ or 3+) and/or Golgi staining seen in reactive lymphocytes. Acute myeloid leukemia or myeloid LC may occasionally show 1+ (and rarely 2-3+) cytoplasmic/membranous or nonspecific blush nuclear CD30 labeling. Strong diffuse staining for CD30 should prompt consideration of a reactive lymphoid/lymphoproliferative process, and, when the clinical likelihood of CD30 LC is low, may obviate the need for further immunohistochemistry.
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