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. 2015 Jan 27;2015:230846. doi: 10.1155/2015/230846

Table 1.

Details of patients with pulmonary hypertension after chemotherapy.

Case Age, sex Neoplasm Treatment for neoplasm Period from chemotherapy to PH onset Clinical diagnosis [cause of death] Pathological findings Lung specimen
1 46, M Malignant lymphoma Surgical resection +
chemotherapy
8 years IP In situ thrombosis of SPA and veins Biopsy
2 6, F NB Surgical resection +
AutoPBSCT (2) + high-dose chemotherapy
7 days IP, PVOD In situ thrombosis of SPA and veins Biopsy
3 2, F ALL Umbilical cord blood transplant (2) + high-dose chemotherapy 10 days PAH,
Congenital protein C deficiency
In situ thrombosis of SPA Biopsy
4 2, M RMS Chemotherapy +
Proton therapy
During chemotherapy Hepatic venoocclusive disease [unknown] In situ thrombosis of SPA and veins Autopsy
5 5, M Burkitt's
Lymphoma
Chemotherapy During chemotherapy PVOD [refractory right HF] PVOD Autopsy
6 3, M MB Surgical resection +
chemotherapy
9 months s/o PAH, PVOD
[IP]
IPAH, IP Autopsy
7 2, F AML Allogeneic bone marrow transplant + high-dose chemotherapy 2 months s/o PVOD, cGVHD [IP] Plexogenic arteriopathy, IP Autopsy

ALL = acute lymphocytic leukemia; AML = acute myelogenous leukemia; AutoPBSCT = autologous peripheral blood stem cell transplantation; cGVHD = chronic graft versus host disease; F = female; HF = heart failure; IP = interstitial pneumonia; IPAH = idiopathic pulmonary arterial hypertension; M = male; MB = medulloblastoma; NB = neuroblastoma; PAH = pulmonary arterial hypertension; PH = pulmonary hypertension; PVOD = pulmonary venoocclusive disease; RMS = rhabdomyosarcoma; SPA = small pulmonary arteries.