WEN-CHUN CHANGBOR-CHING SHEURUEY-JIEN CHENSONG-NAN CHOWHuang S.-C.2021-02-032021-02-0320041048-891Xhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-4544295681&doi=10.1111%2fj.1048-891X.2004.014547.x&partnerID=40&md5=7ee57b0e2feff54cc6e48433b23ab037https://scholars.lib.ntu.edu.tw/handle/123456789/546105Metachronous primary malignant tumors of uterine papillary serous carcinoma (UPSC) and non-Hodgkin's lymphoma (NHL) are rare. UPSC is a clinically aggressive and morphologically distinctive variant of endometrial carcinoma. We describe the clinical features of a 63-year-old patient with UPSC that was found 2 years after chemotherapy for malignant lymphoma of neck, stage IV and 5 months after radiation therapy for recurrence. This patient had undergone staging surgery and postoperative radiation for UPSC. One month after completion of radiotherapy, the patient expired due to persistence of the disease. The association between host immunity and UPSC is rarely described in the literature. Immunological profiles of this patient, with compositional changes of natural killer, B, and T cell, dramatically altered the percentage of CD4+ T cell, CD8+ T cell, and CD4/CD8 ratio, signifying depressed host immunity. Immunological profile of this patient stressed the issue of depressed host immunity and associated malignancies.[SDGs]SDG3antineoplastic agent; CD4 antigen; CD8 antigen; adult; article; case report; clinical feature; disease association; endometrium carcinoma; female; flow cytometry; human; immunity; medical literature; natural killer cell; nonhodgkin lymphoma; papillary carcinoma; postoperative period; priority journal; recurrent disease; uterine papillary serous carcinoma; uterus carcinoma; Carcinoma, Papillary; Disease Progression; Female; Flow Cytometry; Humans; Immunocompromised Host; Killer Cells, Natural; Lymphoma, Non-Hodgkin; Middle Aged; Neoplasms, Second Primary; T-Lymphocytes; Uterine NeoplasmsDepressed host immunity in a case of metachronous primary uterine papillary serous carcinoma and non-Hodgkin's lymphomajournal article10.1111/j.1048-891X.2004.014547.x153612202-s2.0-4544295681