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1.
Transplant Proc ; 50(8): 2553-2557, 2018 Oct.
Article in English | MEDLINE | ID: mdl-30316397

ABSTRACT

BACKGROUND: Condyloma acuminatum (CA) is a common sexually transmitted disease associated with human papilloma virus (HPV). CA occurring in the urethra is rare and has not been reported in male renal transplant recipients. In addition, despite immunosuppressive conditions and increased risk of HPV-related malignant neoplasms in transplant recipients, HPV testing in male transplant recipients has been uncommon. Here we report a case of urethral CA in a male deceased donor renal transplantation recipient and discuss the importance of HPV testing in male transplant recipients. CASE PRESENTATION: A 33-year-old male deceased donor renal transplant recipient presented with miction pain 5 years after the transplantation. He reported repeated urinary tract infections with no sexual contact since the renal transplantation. Multiple papillary tumors in his penile urethra were detected by cystoscopy, and a biopsy sample was pathologically diagnosed with CA. Transurethral tumor resection was performed, and the tumors were completely resected. Additional HPV risk type screening with a urethral smear sample showed the prevalence of low-risk HPV. Although tacrolimus was switched to everolimus and imiquimod cream was administered, the tumors recurred 6 months after the resection, and a second resection was performed. No further recurrence has been observed for 1 year to date. CONCLUSION: As the urethral CA was possibly related to immunosuppressive conditions and a risk for HPV-related malignant neoplasm, the case required careful diagnosis, including HPV risk type. The methodology of sampling for HPV testing in men has not been established. This case suggests the necessity for further discussion about HPV testing in male transplant recipients.


Subject(s)
Condylomata Acuminata/immunology , Immunocompromised Host/immunology , Kidney Transplantation/adverse effects , Urethral Diseases/immunology , Adult , Everolimus/therapeutic use , Humans , Imiquimod/therapeutic use , Immunosuppressive Agents/therapeutic use , Male , Tacrolimus/therapeutic use , Transplant Recipients
2.
Transplant Proc ; 50(3): 898-901, 2018 Apr.
Article in English | MEDLINE | ID: mdl-29661460

ABSTRACT

BACKGROUND: Paraganglioma (extra-adrenal pheochromocytoma) of the bladder is a very rare disease, accounting for 0.06% of all bladder tumors. Optimal management of bladder paraganglioma before kidney transplantation is unknown. We report a case of partial cystectomy for urinary bladder paraganglioma before living kidney transplantation. CASE PRESENTATION: A 59-year-old man with a 27-year history of hemodialysis was referred to our department for further examination of a bladder tumor detected during pre-transplantation testing. Cystoscopy revealed a submucosal tumor on the right side of the bladder. The patient experienced a hypertensive crisis during transurethral resection of the bladder tumor. Endocrinologic and pathologic examinations confirmed the diagnosis of paraganglioma in the urinary bladder. A partial cystectomy was performed before kidney transplantation. Nine months after partial cystectomy, the patient underwent AB0-incompatible living kidney transplantation from his spouse. No disease recurrence or graft rejection was observed 12 months after the transplantation. CONCLUSIONS: To our knowledge, this is the 1st report on the management of paraganglioma in the urinary bladder before living kidney transplantation. Kidney transplantation after partial cystectomy is an option that may be considered in patients with paraganglioma of the urinary bladder, with careful observations of bladder function and vesicoureteral reflux to the grafts.


Subject(s)
Kidney Transplantation , Paraganglioma/complications , Paraganglioma/surgery , Urinary Bladder Neoplasms/complications , Urinary Bladder Neoplasms/surgery , Adult , Cystectomy/methods , Humans , Kidney Failure, Chronic/complications , Kidney Failure, Chronic/surgery , Male , Middle Aged
3.
Transplant Proc ; 46(5): 1371-6, 2014 Jun.
Article in English | MEDLINE | ID: mdl-24836837

ABSTRACT

There are few reports about the quality of life (QOL) and morbidities of pediatric living donor liver transplantation (LDLT) donors. We evaluated the potential morbidities and identified the predictive factors regarding the QOL of living donors after pediatric LDLT. This cross-sectional study was a single-center analysis of 100 donors for pediatric LDLT. The severity of morbidities was assessed with the Clavien classification, the QOL was investigated with the short form-36 (SF-36), and the decision-making process regarding donation was analyzed with questionnaires. The median follow-up period was 3.8 years (range, 2.2-6.0 years). A total of 13% of the donors developed postoperative complications of Clavien grades I (7%), II (3%), and IIIA (3%). There was no grade IV morbidity or mortality. Eighty-one donors responded to the questionnaire and SF-36. The analysis of the questionnaires revealed that the donors had difficulty in the decision-making process, and suggested that it may be necessary to administer multistep informed consent. We identified unique predictive risk factors for lower SF-36 scores in the donors, which were the time to donation (more than 4 weeks) and the predonation self-oriented perception. The donors who have risk factors require enhanced pre- and post-donation psychological care.


Subject(s)
Liver Transplantation , Living Donors , Quality of Life , Adult , Child , Cross-Sectional Studies , Humans , Treatment Outcome
4.
Acta Paediatr Jpn ; 31(6): 745-7, 1989 Dec.
Article in English | MEDLINE | ID: mdl-2576174

ABSTRACT

(1) This is the first study to demonstrate that CSF 5HTP, HVA and DOPAC of asphyxiated newborns are higher than those of healthy newborn infants. (2) This study shows Neurochem, a newly developed neurochemical analyzer, is useful equipment in neonatal neurological research.


Subject(s)
Asphyxia Neonatorum/cerebrospinal fluid , Neurotransmitter Agents/cerebrospinal fluid , Humans , Infant, Newborn
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