Internal Medicine
Online ISSN : 1349-7235
Print ISSN : 0918-2918
ISSN-L : 0918-2918
Volume 38, Issue 3
Displaying 1-23 of 23 articles from this issue
  • Ken HARUMA
    1999 Volume 38 Issue 3 Pages 217-218
    Published: 1999
    Released on J-STAGE: March 27, 2006
    JOURNAL FREE ACCESS
    Download PDF (290K)
  • Norihiro KAMINAGA, Adolfo PARRA-BLANCO, Rikiya FUJITA
    1999 Volume 38 Issue 3 Pages 219-220
    Published: 1999
    Released on J-STAGE: March 27, 2006
    JOURNAL FREE ACCESS
    Download PDF (272K)
  • Harukata KATANO, Tetsutaro SATA
    1999 Volume 38 Issue 3 Pages 221-222
    Published: 1999
    Released on J-STAGE: March 27, 2006
    JOURNAL FREE ACCESS
    Download PDF (246K)
  • Koji ABE
    1999 Volume 38 Issue 3 Pages 223
    Published: 1999
    Released on J-STAGE: March 27, 2006
    JOURNAL FREE ACCESS
    Download PDF (206K)
  • Takashi OKAMURA, Yoshiyuki NIHO
    1999 Volume 38 Issue 3 Pages 224-225
    Published: 1999
    Released on J-STAGE: March 27, 2006
    JOURNAL FREE ACCESS
    Download PDF (233K)
  • Fujio NUMANO, Yasushi KOBAYASHI
    1999 Volume 38 Issue 3 Pages 226-232
    Published: 1999
    Released on J-STAGE: March 27, 2006
    JOURNAL FREE ACCESS
    Download PDF (2868K)
  • C. H. EVANS, P. D. ROBBINS
    1999 Volume 38 Issue 3 Pages 233-239
    Published: 1999
    Released on J-STAGE: March 27, 2006
    JOURNAL FREE ACCESS
    Genes encoding anti-arthritic products can be transferred to intra-or extraarticular sites where their expression suppresses various aspects of the pathophysiology of arthritis. A variety of viral and non-viral vectors can be used for the in vivo or ex vivo delivery of such genes. Promising pre-clinical data have resulted from the application of these strategies in several animal models of disease. Genes showing efficacy in this way include thise encoding interleukin (IL) -1Ra, IL-1sR, TNFsR, transforming growth factor β (TGF-β), IL-13, Fas L, IL- 10 and vIL-10. Two human arthritis gene therapy protocols are underway in the USA and Germany. Both studies involve the ex vivo transfer of an IL-1Ra cDNA to the metacarpophalangeal joints of patients with rheumatoid arthritis. Progress in developing gene treatments for arthritis has been rapid, and permits optimism about their ability eventually to improve the treatment of this group of diseases.
    (Internal Medicine 38: 233-239, 1999)
    Download PDF (1493K)
  • Takafumi YAMAMOTO, Jun MATSUMOTO, Ken SHIOTA, Shin-ichi KITAJIMA, Masa ...
    1999 Volume 38 Issue 3 Pages 240-243
    Published: 1999
    Released on J-STAGE: March 27, 2006
    JOURNAL FREE ACCESS
    The spiral bacteria, Helicobacter heilmannii (H.heilmannii), distinct from Helicobacter pylori (H. pylori), was found in the gastric mucosa of a 71-year-old man without clinical symptoms. The endoscopic examination revealed erosive gastritis. Rapid urease test from the antral specimen was positive, but both culture and immunohistological staining for H.pylori were negative. Touch smear cytology showed tightly spiral bacteria, which were consistent with H.heilmannii. At the second endoscopy after medication regimen for eradication of H. pylori, inflammation was decreased and the rapid urease test was negative. The second cytology showed no evidence of H.heilmannii. Anti-H.pylori therapy may be a useful medication for H.heilmannii.
    (Internal Medicine 38: 240-243, 1999)
    Download PDF (2156K)
  • Naoto SATO, Hiromasa OHIRA, Hiroshi ORIKASA, Jotaro SHINZAWA, Tomohiro ...
    1999 Volume 38 Issue 3 Pages 244-248
    Published: 1999
    Released on J-STAGE: March 27, 2006
    JOURNAL FREE ACCESS
    A case of anti-mitochondrial antibody (AMA)-negative primary biliary cirrhosis (PBC) associated with painless thyroiditis is reported in a 47-year-old woman who diagnosed as PBC based on her elevated serum γ-glutamyl transpeptidase and immunoglobulin M levels, as well as histological findings of destroyed bile ducts surrounded by mononuclear infiltrates in the biopsied liver. She was negative for AMA and had a depressed level of thyroid-stimulating hormone accompanied by increased free thyrosine, thyroxine and triiodothyronine levels and low titers of anti-microsomal and anti-thyroid peroxidase antibodies. Her thyroid disorder corresponded with painless thyroiditis. An association between PBC and hyperthyroidism is rare. Furthermore, an association between AMA-negative PBC and hyperthyroidism due to painless thyroiditis has not previously been reported.
    (Internal Medicine 38: 244-248, 1999)
    Download PDF (1057K)
  • Hiroshi NAKASE, Toshinao ITANI, Jun MIMURA, Toshihiko KAWASAKI, Hidesh ...
    1999 Volume 38 Issue 3 Pages 249-251
    Published: 1999
    Released on J-STAGE: March 27, 2006
    JOURNAL FREE ACCESS
    A 54-year-old female with chronic headache was admitted to our hospital because of hematochezia. She had routinely taken loxoprofen sodium because of severe headache. Emergent colonoscopic examination revealed ulceration of the cecum. After administration of loxoprofen sodium was discontinued and administration of sulfasalazine was initiated, her intestinal bleeding subsided. Two months after discontinuation of loxoprofen sodium, the colonoscopic examination revealed scar formation at the site of cecal ulceration. In this case, it was conceivable that the administration of loxoprofen sodium might have induced colonic ulceration.
    (Internal Medicine 38: 249-251, 1999)
    Download PDF (1470K)
  • Toshiya AIZAKI, Manabu OSAKA, Hideyuki HARA, Shingo KUROKAWA, Kotaro M ...
    1999 Volume 38 Issue 3 Pages 252-256
    Published: 1999
    Released on J-STAGE: March 27, 2006
    JOURNAL FREE ACCESS
    A 61-year-old woman developed hypokalemia, atrioventricular block and ventricular tachycardia with syncope after habitual drinking 2 to 3 liters of oolong tea per day. She had been suffering from rheumatoid arthritis and Sjögren's syndrome and her serum albumin was decreased (2.9 g/dl). Oolong tea contains caffeine at approximately 20 mg/dl. Great quantities of caffeine can induce hypokalemia. The serum protein binding caffeine is albumin. Accordingly, in patients with hypoalbuminemia, caffeine is apt to induce hypokalemia. This case suggested that great quantities of oolong tea, one of the so-called "healthy" drinks, result in serious symptoms for patients with hypoalbuminemia.
    (Internal Medicine 38: 252-256, 1999)
    Download PDF (2661K)
  • Fumio OKAMURA, Atsushi TASHIRO, Atsushi UTSUMI, Towako IMAI, Takatoshi ...
    1999 Volume 38 Issue 3 Pages 257-260
    Published: 1999
    Released on J-STAGE: March 27, 2006
    JOURNAL FREE ACCESS
    It has been reported that depression and diabetes mellitus often occur together, and insulin resistance has been observed in patients with depression. For further understanding of the relationship of depression to insulin resistance, three patients with depression were given the oral glucose tolerance test (OGTT) and the frequently sampled intravenous glucose tolerance test (FSIGT) with minimal model analysis before and after antidepressant treatment. Depressive patients showed decreased glucose tolerance, enhanced insulin secretion, and diminished insulin sensitively during OGTT and FSIGT. These abnormalities were resolved after their recovery from depression without changes in body weight or diet.
    (Internal Medicine 38: 257-260, 1999)
    Download PDF (791K)
  • Yasunari JIN-NO, Yoshinobu KAMIYA, Masami OKADA, Makoto HIRAKO, Norio ...
    1999 Volume 38 Issue 3 Pages 261-265
    Published: 1999
    Released on J-STAGE: March 27, 2006
    JOURNAL FREE ACCESS
    Isolated magnesium malabsorption is a rare disorder, which has been described in no more than 30 patients worldwide. Patients with this disorder typically present with convulsion and diarrhea in early infancy. Hypomagnesemia and hypocalcemia were found in a 35-year-old man with muscle cramps, who bad been diagnosed as primary hypoparathyroidism. Oral magnesium therapy corrected the low serum calcium, magnesium and parathyroid hormone levels. We report an atypical case of isolated magnesium malabsorption in an adult.
    (Internal Medicine 38: 261-265, 1999)
    Download PDF (856K)
  • Noriyoshi YAMAKITA, Takashi KOMAKI, Toshihiro MURAI, Satoru KAWAMURA
    1999 Volume 38 Issue 3 Pages 266-271
    Published: 1999
    Released on J-STAGE: March 27, 2006
    JOURNAL FREE ACCESS
    A pituitary tumor with suprasellar extension was found by magnetic resonance imaging (MRI) in a male with diabetes mellitus. Endocrine examination revealed high plasma follicle-stimulating hormone (FSH) and α-subunit levels, which increased with administration of thyrotropin (TSH)-releasing hormone (TRH). Plasma luteinizing hormone (LH) and testosterone levels were low. Pituitary gonadotropin producing tumor was diagnosed. Because the patient refused surgery, bromocriptine was administered and plasma FSH and α-subunit rapidly decreased; on MRI the tumor size was gradually reduced. When pituitary operation is not feasible, bromocriptine is one choice of treatment.
    (Internal Medicine 38: 266-271, 1999)
    Download PDF (1674K)
  • Terumasa HAYASHI, Nakaya SAITO, Tatsuya SHOJI, Masaki TOGAWA, Noriyuki ...
    1999 Volume 38 Issue 3 Pages 272-275
    Published: 1999
    Released on J-STAGE: March 27, 2006
    JOURNAL FREE ACCESS
    We describe three cases of nephrotic syndrome with a contra-indication for steroid therapy successfully treated with cyclosporin A (CsA). A 21-year-old man with focal segmental glomerulosclerosis (FSGS) complicated by necrosis of the femoral head, and a 34-year-old woman and a 48-year-old man with minimal change disease (MCD) complicated by psychogenic reaction and diabetes mellitus, respectively, were given CsA at initial dosages of 3.8-5.0 mg/kg/day and immediately remitted completely. However, two of these patients suffered relapses when CsA was tapered. They are currently maintained in complete or partial remission on CsA at dosages of 3.2-4.7 mg/kg/day. These findings suggest that CsA mono-therapy may be useful in nephrotic syndrome patients contra-indicated for steroid therapy.
    (Internal Medicine 38: 272-275, 1999)
    Download PDF (625K)
  • Junji TSURUTANI, Akitoshi KINOSHITA, Hideyuki KAIDA, Hideharu FUJII, F ...
    1999 Volume 38 Issue 3 Pages 276-278
    Published: 1999
    Released on J-STAGE: March 27, 2006
    JOURNAL FREE ACCESS
    The tracheal tumor of a 74-year-old female was detected on bronchscopy and histologically diagnosed as mucosa-associated lymphoid tissue (MALT) lymphoma. We successfully treated the tumor with endoscopic neodyminum-yttruim-aluminium-garnet (Nd-YAG) laser photoresection followed by local el Hanoi injection. This is the first case in which tracheal MALT lymphoma was successfully treated with bronchoscopy. Bronchoscopic therapy seems to be one of the most valuable strategies for treatment of MALT lymphomas of the central airway.
    (Internal Medicine 38: 276-278, 1999)
    Download PDF (1345K)
  • Mitsutoshi HAYASHI, Kazutetsu AOSHIBA, Masahiko SHIMADA, Yutaka IZAWA, ...
    1999 Volume 38 Issue 3 Pages 279-282
    Published: 1999
    Released on J-STAGE: March 27, 2006
    JOURNAL FREE ACCESS
    A 32-year-old female was admitted for evaluation of multiple infiltrates on a chest radiograph. A diagnosis of multicentric Castleman's disease was made on the basis of typical clinical manifestations. Transbronchial lung biopsy (TBLB) revealed histological findings reported in lymphocytic interstitial pneumonia. Both the polymerase chain reaction and in situ hybridization with a probe specific for Kaposi's sarcoma-associated herpesvirus (KSHV) sequences demonstrated the presence of KSHV in the TBLB sample.
    (Internal Medicine 38: 279-282, 1999)
    Download PDF (2399K)
  • Kazuro SUGISHITA, Hiroyuki NAGASE, Toshiyuki TAKAHASHI, Katsu TAKENAKA ...
    1999 Volume 38 Issue 3 Pages 283-286
    Published: 1999
    Released on J-STAGE: March 27, 2006
    JOURNAL FREE ACCESS
    Production of coagulation factor VIII inhibitor is rarely encountered in non-hemophilic patients. A 63-year-old Japanese male suffered from severe bleeding tendency caused by this inhibitor. Although he did not have malignancy or collagen disease, he had chronic hepatitis C virus (HCV) infection. Although HCV is known to induce production of various autoimmune antibodies, this may be the first report of a case with both acquired factor VIII inhibitor and HCV infection.
    (Internal Medicine 38: 283-286, 1999)
    Download PDF (703K)
  • Manabu HATTORI, Hiroyuki YUASA, Koji TAKADA, Tomoyuki YAMADA, Kentaro ...
    1999 Volume 38 Issue 3 Pages 287-289
    Published: 1999
    Released on J-STAGE: March 27, 2006
    JOURNAL FREE ACCESS
    Dentatorubral-pallidoluysian atrophy (DRPLA) is associated with an unstable CAG trinucleotide sequence. We describe a DRPLA family whose members have an allele containing an expanded CAG repeat, even in an elderly neurologically normal individual. The proband developed DRPLA at age 14. She was initially considered a sporadic case, but later her sister became symptomatic. Investigation of the number of CAG repeat units in her family revealed the 81-year-old father to have an expanded CAG repeat of 51 units. To our knowledge, such an advanced aged unaffected patient has not been previously documented. The present example may explain apparent sporadic cases.
    (Internal Medicine 38: 287-289, 1999)
    Download PDF (1045K)
  • Masatoshi YOSHINO, Yuzo YOSHIMI, Masayuki TANIGUCHI, Saburo NAKAMURA, ...
    1999 Volume 38 Issue 3 Pages 290-292
    Published: 1999
    Released on J-STAGE: March 27, 2006
    JOURNAL FREE ACCESS
    A 79-year-old woman suffering from urinary incontinence and unsteady gait was diagnosed as having idiopathic normal pressure hydrocephalus (NPH) with hyponatremia due to the syndrome of inappropriate secretion of antidiuretic hormone (SIADH). The concentration of antidiuretic hormone was high while the plasma osmolality was low in the presence of concentrated urine during the episodes of hyponatremia. Magnetic resonance imaging (MRI) of the head showed enlargement of the third and lateral ventricles. After ventriculoperitoneal shunt surgery, the symptoms of NPH and hyponatremia improved. It may be possibly explained that mechanical pressure on the hypothalamus from the third ventricle is responsible for hyponatremia.
    (Internal Medicine 38: 290-292, 1999)
    Download PDF (1646K)
  • Masanaka TAKEDA, Hisao TACHIBANA, Naomi SHIBUYA, Yatuka NAKAJIMA, Bung ...
    1999 Volume 38 Issue 3 Pages 293-295
    Published: 1999
    Released on J-STAGE: March 27, 2006
    JOURNAL FREE ACCESS
    There have been few case reports of pure anomic aphasia and the underlying mechanism remains to be clarified. We report a patient in whom pure anomic aphasia was caused by subcortical hemorrhage in the left temporo-parieto-occipital lobe. Based on magnetic resonance images and cerebral blood flow imaging, the structural lesion underlying the pure anomic aphasia was thought to be located at the left temporo-occipital junction.
    (Internal Medicine 38: 293-295, 1999)
    Download PDF (1740K)
  • Masayuki ITO, Hiromasa OHIRA, Masayuki MIYATA, Tomohiro SUZUKI, Yukio ...
    1999 Volume 38 Issue 3 Pages 296-301
    Published: 1999
    Released on J-STAGE: March 27, 2006
    JOURNAL FREE ACCESS
    In a 31-year-old Japanese man with cytophagic histiocytic panniculitis (CHP) remission was achieved by a combination of combined chemotherapy CHOP and cyclosporin A treatment. He was admitted to our hospital in January 1994 with recurrent high fever of 40.2° and tender and violaceous subcutaneous nodules on his trunk, arms and legs. He developed pancytopenia, hemorrhagic diathesis, liver dysfunction. Histological examination of the biopsied subcutaneous nodule revealed a lobular panniculitis with fat necrosis and a massive infiltration of histiocytes phagocytosing nuclear debris. He was treated initially with 40 mg/day prednisolone. However, following a reduction in prednisolone dosage, his symptoms reappeared. CHOP (cyclophosphamide, doxorubicin, vincristine and prednisolone) therapy was then initiated. Three courses of CHOP treatment alleviated his symptoms and cyclosporin A was used to maintain his condition for 15 months. His medication was then discontinued and he has been in complete remission for 10 months. Combined treatment of cyclosporin A and CHOP combined chemotherapy was shown to be effective for this patient with severe CHP.
    (Internal Medicine 38: 296-301, 1999)
    Download PDF (2347K)
  • Miwako HONDA, Akira YASUOKA, Makoto AOKI, Shinichi OKA
    1999 Volume 38 Issue 3 Pages 302-303
    Published: 1999
    Released on J-STAGE: March 27, 2006
    JOURNAL FREE ACCESS
    Nelfinavir, one of human immunodeficiency virus (HIV) specific protease inhibitors(PIs), is widely used for the treatment of HIV infection. Nelfinavir, which is metabolized with the cytochrome p450 isoforms, elevate the phenytoin level theoretically because nelfinavir acts as an inhibitor of phenytoin metabolism through the enzyme. However, we encountered a case of seizure recurrence caused by a lowered phenytoin level after initiation of nelfinavir. We should be aware of the change in the phenytoin level in concomitant use of nelfinavir.
    (Internal Medicine 38: 302-303, 1999)
    Download PDF (424K)
feedback
Top