2000
DOI: 10.1016/s0190-9622(00)90273-1
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Cutaneous presentation of posttransplant lymphoproliferative disorder

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Cited by 36 publications
(32 citation statements)
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“…Cutaneous PTLD behaves less aggressively than identical extracutaneous lesions. 3,[7][8][9][10][11] PTLD can also be classified by pathology. The morphologic categories of PTLD include plasmacytic hyperplasia/infectious mononucleosis-like PTLD, polymorphic PTLD, monomorphic B-cell PTLD, monomorphic T-cell PTLD, and Hodgkin lymphoma/Hodgkin lymphoma-like PTLD.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Cutaneous PTLD behaves less aggressively than identical extracutaneous lesions. 3,[7][8][9][10][11] PTLD can also be classified by pathology. The morphologic categories of PTLD include plasmacytic hyperplasia/infectious mononucleosis-like PTLD, polymorphic PTLD, monomorphic B-cell PTLD, monomorphic T-cell PTLD, and Hodgkin lymphoma/Hodgkin lymphoma-like PTLD.…”
Section: Discussionmentioning
confidence: 99%
“…Previously reported cases have been treated by reduction of immunosuppression, surgery, or radiotherapy, with good clinical outcomes. 3,[7][8][9][10][11] Our patient responded completely to a reduction of immunosuppression with no evidence of recurrence or metastasis 2 years later. …”
Section: Discussionmentioning
confidence: 99%
“…Clinical features including initial disease for transplant, time to PTLD, site of PTLD, stage of the patient, recurrence, immunosuppression regimen, and type and response to treatment, were evaluated for all PTLDs. One LTx patient (Patient 3) was previously reported (25). Autopsies were performed in five cases (1 LTx patient and 4 non-LTx patients).…”
Section: Methodsmentioning
confidence: 99%
“…When they do occur, skin lesions of PTLD present as solitary or multiple nontender erythematous nodules, exophytic tumors, ulcers, indurated plaques, or maculopapules, with reported areas of involvement including the forehead, lower lip, upper and lower extremities, and trunk. [16][17][18][19][20][21][22][23][24][25][26][27][28] Finally, an angiocentric and angioinvasive lymphocytic infiltrate has, to our knowledge, been associated only once with PTLD, in a case that also showed features of LYG. 29 Our patient also presented with features suggestive of LYG, including lesions in the skin and lungs and an EBV-positive angiocentric and angioinvasive lymphocytic infiltrate.…”
Section: Discussionmentioning
confidence: 99%