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Development of an AI-Assisted Diagnostic Tool for Mycosis Fungoides and Other Cutaneous Lymphoproliferative Diseases Using Microscopic Image Analysis: A Training and Validation Study

2026년 7월 14일 업데이트: Kariman Mostafa Sayed Mansour, Cairo University

Cutaneous lymphoproliferative diseases (CLPDs) are a group of skin disorders that range from benign conditions, such as pseudolymphomas, to malignant forms like cutaneous T-cell and B-cell lymphomas. Mycosis fungoides is the most common malignant type, but diagnosis is often difficult because many benign skin conditions can mimic lymphoma. Current diagnostic methods rely on microscopic examination of biopsies, which can be subjective and vary between pathologists.

This study aims to develop and validate a deep learning model that uses digitized biopsy images and clinical data to distinguish malignant CLPDs from benign ones. By applying artificial intelligence to dermatopathology, the project seeks to improve diagnostic accuracy, reduce variability, and support clinicians in making timely treatment decisions. The novelty of this work lies in applying advanced AI methods to a rare and challenging group of skin diseases, with the potential to enhance patient care in both specialized centers and resource-limited settings.

연구 개요

상세 설명

Cutaneous lymphoproliferative diseases (CLPDs) encompass both benign and malignant disorders, ranging from pseudolymphomas to cutaneous T-cell and B-cell lymphomas. Mycosis fungoides (MF) is the most common malignant subtype, but diagnosis is often challenging because benign inflammatory conditions can closely mimic lymphoma. Histopathological examination remains the gold standard, yet interpretation is subjective and prone to inter-observer variability. This highlights the need for standardized diagnostic tools, including artificial intelligence (AI) solutions.

This study is a retrospective diagnostic accuracy investigation using routinely collected data. Archived hematoxylin and eosin (H&E) stained slides of patients with MF and other CLPDs will be retrieved from the Dermatopathology Unit at Kasr Al-Aini Hospitals, Cairo University. Slides of benign mimickers such as pseudolymphoma and pityriasis lichenoides will also be included. Cases with poor slide quality or insufficient data will be excluded.

Digitized images will be captured using both high-resolution microscope cameras and standardized smartphone devices to evaluate feasibility. Experienced dermatopathologists will annotate regions of interest, and relevant clinical data will be extracted to build a structured database. Deep learning models, particularly convolutional neural networks (CNNs), will be trained and validated on these datasets. Preprocessing techniques such as color normalization, stain separation, and data augmentation will be applied to enhance robustness.

The primary outcomes are diagnostic accuracy, sensitivity, specificity, and predictive values of the AI models in differentiating malignant from benign CLPDs, and in staging MF. Secondary outcomes include comparison with expert dermatopathologists, assessment of smartphone-based imaging, and evaluation across magnification levels. More than 500 slides collected over the past five years will be used, divided into training, validation, and testing sets.

By integrating AI into dermatopathology, this study aims to reduce diagnostic variability, improve accuracy, and explore novel imaging approaches. The work represents one of the first applications of deep learning to CLPDs, with potential to enhance patient care in both specialized centers and resource-limited healthcare settings.

연구 유형

관찰

등록 (추정된)

463

연락처 및 위치

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연구 장소

      • Cairo, 이집트
        • Kasr Al-Aini Hospitals, Cairo University

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 어린이
  • 성인
  • 고령자

건강한 자원 봉사자를 받아들입니다

해당 없음

샘플링 방법

비확률 샘플

연구 인구

Archived slides of patients diagnosed with malignant CLPDs (e.g., mycosis fungoides, cutaneous B-cell lymphoma) and benign mimickers (e.g., pseudolymphoma, pityriasis lichenoides chronica, PLEVA) were identified from the pathology database of Kasr Al-Aini Hospitals, Cairo University.

Cases were selected based on WHO-EORTC diagnostic criteria and availability of adequate quality H&E slides plus relevant clinical data.

설명

Inclusion Criteria:

  • Archived slides of patients with a confirmed histopathological diagnosis of malignant CLPDs (e.g., mycosis fungoides at all stages, cutaneous B-cell lymphoma, primary cutaneous anaplastic large cell lymphoma, lymphomatoid papulosis), based on WHO-EORTC criteria.
  • Archived slides of patients with benign CLPDs that mimic MF clinically and histologically (e.g., pseudolymphoma, pityriasis lichenoides chronica, pityriasis lichenoides et varioliformis acuta [PLEVA]).
  • Availability of adequate quality hematoxylin and eosin (H&E) stained slides.
  • Availability of relevant clinical data (age, sex, disease duration, distribution of lesions, drug history).

Exclusion Criteria:

  • Slides with significant artifacts (folding, tearing, poor staining) that prevent adequate image analysis.
  • Cases with insufficient clinical or pathological data for definitive diagnosis.
  • Cases with secondary cutaneous CLPDs

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

코호트 및 개입

그룹/코호트
개입 / 치료
MF
Patients diagnosed histopathologically as mycosis fungoides

Development and validation of a deep learning model using digitized hematoxylin and eosin (H&E) stained slides and clinical data to differentiate malignant CLPDs from benign mimickers.

Comparator: Standard histopathological diagnosis by experienced dermatopathologists.

PLC/PLEVA
Patients diagnosed histopathologically as PLC or PLEVA

Development and validation of a deep learning model using digitized hematoxylin and eosin (H&E) stained slides and clinical data to differentiate malignant CLPDs from benign mimickers.

Comparator: Standard histopathological diagnosis by experienced dermatopathologists.

TCD
Patients diagnosed histopathologically as T cell dyscrasia

Development and validation of a deep learning model using digitized hematoxylin and eosin (H&E) stained slides and clinical data to differentiate malignant CLPDs from benign mimickers.

Comparator: Standard histopathological diagnosis by experienced dermatopathologists.

BCL
Patients diagnosed histopathologically as B cell lymphoma

Development and validation of a deep learning model using digitized hematoxylin and eosin (H&E) stained slides and clinical data to differentiate malignant CLPDs from benign mimickers.

Comparator: Standard histopathological diagnosis by experienced dermatopathologists.

Pseudolymphoma
Patients diagnosed histopathologically as pseudo lymphoma

Development and validation of a deep learning model using digitized hematoxylin and eosin (H&E) stained slides and clinical data to differentiate malignant CLPDs from benign mimickers.

Comparator: Standard histopathological diagnosis by experienced dermatopathologists.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Diagnostic accuracy of AI model
기간: Baseline (In retrospective diagnostic studies, the moment the AI evaluates the historical slide is considered the patients's baseline).
Accuracy, sensitivity, specificity, and positive predictive value of the trained AI models in differentiating benign CLPDs from malignant types.
Baseline (In retrospective diagnostic studies, the moment the AI evaluates the historical slide is considered the patients's baseline).

2차 결과 측정

결과 측정
측정값 설명
기간
Comparison with dermatopathologists
기간: Baseline (In retrospective diagnostic studies, the moment the AI evaluates the historical slide is considered the patients's baseline).
Compare AI model diagnostic accuracy with that of experienced dermatopathologists
Baseline (In retrospective diagnostic studies, the moment the AI evaluates the historical slide is considered the patients's baseline).
Smartphone imaging feasibility
기간: Baseline (In retrospective diagnostic studies, the moment the AI evaluates the historical slide is considered the patients's baseline).
Assess feasibility and diagnostic accuracy of AI models using smartphone-captured histopathology images.
Baseline (In retrospective diagnostic studies, the moment the AI evaluates the historical slide is considered the patients's baseline).

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

간행물 및 유용한 링크

연구에 대한 정보 입력을 담당하는 사람이 자발적으로 이러한 간행물을 제공합니다. 이것은 연구와 관련된 모든 것에 관한 것일 수 있습니다.

일반 간행물

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2026년 1월 1일

기본 완료 (추정된)

2026년 11월 30일

연구 완료 (추정된)

2026년 12월 30일

연구 등록 날짜

최초 제출

2026년 6월 30일

QC 기준을 충족하는 최초 제출

2026년 7월 14일

처음 게시됨 (실제)

2026년 7월 15일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 7월 15일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 7월 14일

마지막으로 확인됨

2026년 1월 1일

추가 정보

이 연구와 관련된 용어

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

아니

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AI-assisted histopathology image analysis에 대한 임상 시험

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