CD30 Positive T-Cell Proliferation in Pediatric Skin Conditions - Dermatology

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Primary cutaneous CD30-positive T-cell proliferation


The doctor would like to inquire about a 7-year-old child who had a lump on the clavicle and the outer shoulder two years ago.
After excision and biopsy, the diagnosis was "CD30 positive T-cell proliferation originating in the skin." However, in February of this year, another lump appeared, and the biopsy report was the same.
The oncologist stated it is a malignant tumor, while the dermatologist claims the report indicates it is benign.
Why is there a discrepancy in the interpretations of the same report? A bone marrow biopsy was performed and returned normal results.
Is there a possibility of it progressing to lymphoma?

Cheng, 30~39 year old female. Ask Date: 2017/04/06

Dr. Wu Yuxin reply Dermatology


I cannot provide an answer because I need to see the original pathology report to confirm the details described within it.

Reply Date: 2017/04/06

More Info


Understanding CD30 Positive T-Cell Proliferation in Pediatric Skin Conditions is a complex issue that requires careful consideration of the clinical context, histopathological findings, and the specific characteristics of the lesions involved. In your case, the child has a history of CD30 positive T-cell proliferation, which is a type of lymphoproliferative disorder. This condition can manifest in various forms, including lymphomatoid papulosis and anaplastic large cell lymphoma, both of which can present with similar histological features.

The discrepancy between the opinions of the oncologist and the dermatologist regarding the nature of the lesions—one suggesting malignancy and the other indicating benignity—can be attributed to several factors. First, CD30 positive T-cell proliferation can sometimes be associated with both benign and malignant processes. For instance, lymphomatoid papulosis is considered a benign condition that can have a chronic course, while anaplastic large cell lymphoma is a malignant entity. The distinction between these two can be subtle and may depend on the clinical presentation, the number of lesions, and the patient's overall health.

The fact that the biopsy results are consistent with CD30 positive T-cell proliferation does not automatically classify the condition as malignant. The interpretation of these results can vary based on the clinical context and the specific characteristics of the lesions. For example, if the lesions are solitary, asymptomatic, and have not shown aggressive behavior, they may be viewed as benign. Conversely, if there are multiple lesions, changes in size, or associated systemic symptoms, a more aggressive approach may be warranted.

Regarding the concern about the potential for transformation into lymphatic cancer, it is essential to monitor the child closely. While CD30 positive T-cell proliferation can be associated with a risk of transformation, this is not always the case. The normal bone marrow biopsy results are reassuring, as they suggest that there is no systemic involvement at this time. However, ongoing surveillance is crucial, and any new or changing lesions should be evaluated promptly.

In terms of management, a multidisciplinary approach involving both dermatology and oncology is often beneficial. Regular follow-up appointments should be scheduled to monitor the lesions and assess for any changes. If new lesions develop or if there are changes in the existing lesions, further diagnostic workup may be necessary, including imaging studies or repeat biopsies.

In summary, while the diagnosis of CD30 positive T-cell proliferation can be concerning, it is essential to consider the clinical context and the behavior of the lesions. The differing opinions between specialists highlight the complexity of these cases. Continuous monitoring and a collaborative approach to care will be key in managing this condition effectively. If there are any significant changes or concerns, do not hesitate to seek further evaluation or a second opinion from a specialist experienced in pediatric dermatology and oncology.

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