1.A Case of Paragonimus westermani Infection Diagnosed by Serological Testing
Akihiro Inui ; Toshio Naito ; Eiichiro Sugihara ; Hiroshi Isonuma
General Medicine 2011;12(1):19-23
BACKGROUND: We describe a 40-year-old Thai woman living in Japan who was transferred to Juntendo University Hospital after lung cancer was suspected. Chest X-ray showed a nodular lesion and pleural effusion in the left lung. Laboratory data showed eosinophilia. She denied having consumed raw or undercooked food at the initial interview. Microplate enzyme-linked immunosorbent assay (ELISA) for Paragonimus westermani specific immunoglobulin (Ig) G antibody was positive at a high titer, confirming the diagnosis of P. westermani infection. She was successfully treated with oral praziquantel. All primary practitioners should be aware that paragonimiasis is an important pulmonary disease that can cause nodular lesions on chest X-ray.
2.Polycystic Kidney Complicated by Cholangiocellular Carcinoma Presenting as Fever of Unknown Origin
Nobuhiro Ikeda ; Toshio Naito ; Hiroshi Isonuma ; Takashi Dambara ; Yasuo Hayashida
General Medicine 2005;6(1):23-27
We report the case of a 59-year-old man who presented with classical-type fever of unknown origin (FUO) during observation of hypertension and polycystic kidney. The presence of malignancy was suspected based on elevation of tumor marker levels. We examined the patient carefully and attempted diagnostic imaging, but definitive diagnosis was difficult due to the presence of multiple hepatic cysts. Hepatic biopsy detected adenocarcinoma, but identifying whether lesions were primary cholangiocellular carcinoma or metastases was difficult, and we were ultimately unable to diagnose the tumors as cholangiocellular carcinoma until autopsy. Polycystic kidney with hepatic cysts and complicated by cholangiocellular carcinoma is rare, but should be considered among the differential diagnosis for FUO, which itself is frequently encountered.
3.Overwhelming Pneumococcal Infection Due to Congenital Hyposplenism or Asplenia in Adults
Toshio Naito ; Keiko Kume ; Kazunori Mitsuhashi ; Tetsu Okumura ; Hiroshi Isonuma ; Takashi Dambara ; Koichi Suda ; Yasuo Hayashida
General Medicine 2006;7(1):21-24
We recently encountered a case of fatal pneumococcal infection in a previously healthy 19-year-old female. She had no history of splenectomy, but on autopsy she was found to have hyposplenism. It has been widely reported that life-threatening pneumococcal infection can occur after splenectomy, though cases of hyposplenic or asplenic adults, without a history of splenectomy, are very rare. We report this case and review the literature dealing with 6 similar cases.
4.Malignant Lymphoma of the Ileum
Toshio Naito ; Yukiko Fukuda ; Akihiro Inui ; Naoto Takeda ; Hiroshi Isonuma ; Takashi Dambara ; Yasuo Hayashida
General Medicine 2006;7(1):35-36
5.Acute Retroviral Syndrome Presenting as Infectious Mononucleosis
Toshio Naito ; Nagako Kudo ; Naoko Hada ; Takayoshi Shiga ; Akihiro Inui ; Nobuhiro Ikeda ; Takashi Dambara ; Yasuo Hayashida
General Medicine 2006;7(2):77-80
ABSTRACT: A case of infectious mononucleosis (IM) in a previously healthy 43-year-old male is presented. The patient complained of fever and a sore throat of 3 weeks' duration. Although blood tests showed a marked increase in atypical lymphocytes, tests for Epstein-Barr virus (EBV) and cytomegalovirus (CMV) were negative. Human immunodeficiency virus type 1 (HIV-1) antibody was positive on enzymelinked immunosorbent assay (ELISA), and the HIV-1 viral load was 6.4×104copies/mL. Western blot (WB) analysis did not initially confirm HIV-1 infection ; however, HIV-1 infection was confirmed one month after presentation. Although several pathogens can cause infections presenting as IM, in Japan there have been few reports of acute retroviral syndrome presenting as IM. This case is being reported to stress the importance of the early diagnosis of acute retroviral syndrome.
8.One-Staged Operation for Stanford Type A Aortic Dissection, AAE, Mitral Valve Regurgitation and Pectus Excavatum in a Patient with Marfan's Syndrome.
Chiho Tokunaga ; Tomoaki Jikuya ; Wahei Mihara ; Jun Seita ; Kazuhiro Naito ; Yasushi Terada ; Toshio Mitsui
Japanese Journal of Cardiovascular Surgery 2002;31(4):278-281
A 22-year-old man was hospitalized due to severe back pain having being diagnosed as Stanford type A aortic dissection, AAE, mitral regurgitation and pectus excavatum associated with Marfan's syndrome. A single staged operation including ascending aortic replacement, mitral valve replacement and sternal turnover with a rectus muscle pedicle was carried out in order to keep the blood supply to the plastron to reduce the risk of infection during such a long operation. By this approach, it was found that the operative field was excellent and postoperative hemodynamics were stable. However, frail plastron occurred because of difficulties in keeping the patient stabilized because of severe pain thus re-fixation was required. The necessity of strong pain control after such an operation was also recognized.