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Post-transplantation lymphoproliferative disorder with gastrointestinal involvement
Faisal Inayat1, Ghias Ul Hassan2, Ghias Un Nabi Tayyab2
1Allama Iqbal Medical College, Lahore, Pakistan (Faisal Inayat).
Post-transplantation lymphoproliferative disorders (PTLD) can manifest as aggressive B-cell lymphoma, even in Epstein-Barr virus-negative liver transplant patients. Early endoscopic diagnosis is crucial for gastrointestinal PTLD, which may present without typical symptoms.
Area of Science:
- Transplant medicine
- Oncology
- Virology
Background:
- Post-transplantation lymphoproliferative disorders (PTLD) are common lymphoid tumors in transplant recipients.
- Epstein-Barr virus (EBV) is a major cause of PTLD, particularly in EBV-negative recipients.
- PTLD occurs in 1-3% of liver transplant recipients and presents variably.
Purpose of the Study:
- To report a case of aggressive B-cell lymphoma (PTLD WHO class-3) with isolated gastrointestinal involvement.
- To highlight the diagnostic challenges of EBV-negative PTLD in a liver transplant recipient.
- To emphasize the importance of vigilance for PTLD in transplant patients with gastrointestinal symptoms.
Main Methods:
- Case report of a living-donor liver transplant recipient.
- Diagnosis of aggressive B-cell lymphoma (PTLD WHO class-3) with isolated gastrointestinal involvement.
- EBV-negative status confirmed in the patient.
Main Results:
- The patient developed PTLD 4 years post-transplant.
- The PTLD presented as an aggressive B-cell lymphoma with isolated gastrointestinal manifestation.
- The patient was EBV-negative, complicating typical PTLD diagnosis.
Conclusions:
- Clinicians must maintain a high index of suspicion for PTLD, especially with isolated gastrointestinal involvement in immunocompromised patients.
- Endoscopic evaluation with biopsy is critical for prompt detection and characterization of gastrointestinal PTLD.
- This case underscores the need for vigilance in EBV-negative transplant recipients presenting with atypical symptoms.
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