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1.
Transplant Proc ; 50(3): 947-949, 2018 Apr.
Article in English | MEDLINE | ID: mdl-29661467

ABSTRACT

INTRODUCTION: Tuberculous paradoxical reactions (PRs) are excessive immune reactions occurring after antituberculosis (TB) treatment and are commonly observed in immunocompromised hosts such as patients infected with the human immunodeficiency virus. CASE REPORT: We recently encountered a 63-year-old male heart transplant recipient who developed tuberculous PR after treatment for miliary TB. The patient had been receiving immunosuppressive therapy with cyclosporine and mycophenolate mofetil for over 15 years. The diagnosis of miliary TB was made based on the presence of intermittent fever and fatigue; thus, anti-TB treatments (isoniazid, levofloxacin, ethambutol, and pyrazinamide) were started, which led to rapid defervescence and regression of the granular shadow and pleural effusion. However, a new persistent fever and confused state developed 1 month after the anti-TB therapy was started. After excluding possible etiologies of the patient's symptom, a PR was suspected, and anti-TB drugs were continued; corticosteroids were added as anti-inflammatory agents. After that, he has shown a favorable course with long-term anti-TB chemotherapy. CONCLUSION: A PR should always be considered when the patients' symptoms of tuberculosis re-exacerbate after an appropriate anti-TB therapy. A PR commonly occurs in patients with various immunologic conditions including heart transplant recipients.


Subject(s)
Antitubercular Agents/adverse effects , Heart Transplantation , Postoperative Complications/chemically induced , Tuberculosis, Miliary/drug therapy , Antitubercular Agents/therapeutic use , Cyclosporine/adverse effects , Cyclosporine/therapeutic use , Humans , Immunocompromised Host , Immunosuppressive Agents/therapeutic use , Isoniazid/adverse effects , Isoniazid/therapeutic use , Male , Middle Aged , Postoperative Complications/drug therapy , Postoperative Complications/immunology , Postoperative Complications/microbiology , Tuberculosis, Miliary/immunology , Tuberculosis, Miliary/microbiology
2.
Gerontology ; 48(2): 103-8, 2002.
Article in English | MEDLINE | ID: mdl-11867933

ABSTRACT

OBJECTIVE: To evaluate the efficacy of etidronate (EHDP) on lumbar spine bone mineral density (LSBMD) and total bone mineral density (TBMD) in elderly women with primary hyperparathyroidism (PHPT), we compared changes in LSBMD and TBMD between patients treated by EHDP therapy and parathyroidectomy (PTX). SUBJECTS AND METHODS: Twenty-two PHPT patients were enrolled and randomized into two groups; 9 received EHDP and 13 underwent PTX. All patients were followed up for 1 year by measuring LSBMD, TBMD, serum calcium, inorganic phosphate, parathyroid hormone, 1,25-dihydroxyvitamin D, serum alkaline phosphatase, intact osteocalcin, urinary pyridinoline (U(pyd)) and urinary deoxypyridinoline (U(dpd)). The presence of spinal fractures was evaluated by X-ray photography before and after treatment. RESULTS: EHDP treatment produced a significant increase in LSBMD of 10% compared with pretreatment levels after 1 year (p < 0.03, compared to baseline), while PTX produced a significant increase in LSBMD of 20% compared to pretreatment levels (p < 0.01). However, TBMD remained unchanged for 1 year after both EHDP administration and PTX. Among biochemical bone turnover markers, EHDP administration resulted in significant decreases in alkaline phosphatase by 78%, U(pyd) by 64% and U(dpd) by 37% after 12 months compared with the pretreatment levels (p < 0.05) and intact osteocalcin by 67% after 6 months (p < 0.05). There were no differences in the fracture rate between the EHDP and PTX groups during 1 year. CONCLUSION: EHDP administration results in a somewhat lower increase in LSBMD than that following PTX and suppresses bone formation and resorption in elderly PHPT patients for 1 year. We conclude that PTX is preferable to EHDP therapy for the management of elderly PHPT patients; however, EHDP administration should also be considered for elderly patients with many complications or who are unfit for surgery.


Subject(s)
Etidronic Acid/therapeutic use , Hyperparathyroidism/drug therapy , Hyperparathyroidism/surgery , Parathyroidectomy , Aged , Aged, 80 and over , Biomarkers , Bone Density/drug effects , Bone Remodeling/physiology , Bone Resorption/etiology , Calcium/blood , Female , Hormones/blood , Humans , Hyperparathyroidism/complications , Hyperparathyroidism/physiopathology , Longitudinal Studies , Osteogenesis , Treatment Outcome
3.
Intern Med ; 39(10): 810-3, 2000 Oct.
Article in English | MEDLINE | ID: mdl-11030205

ABSTRACT

A 69-year-old man visited our department of neurology with symptoms of paresthesia on the lower extremities and lumbago. Biochemical examination of serum samples showed hypercalcemia (serum concentration 15.6 mg/dl). The levels of intact parathyroid hormone (i-PTH) and 1,25-dihydroxyvitamin D were suppressed, whereas parathyroid hormone-related peptide (PTHrP) was elevated up to 5.4 pM (normal range: below 0.6 pM). Additionally, bone survey revealed a punched-out lesion in radiological examinations of the skull. Bone marrow aspiration demonstrated many atypical plasma cells suggesting multiple myeloma. Nephrogenous cyclic adenosine monophosphate (cAMP), urinary deoxypyridinoline, plasma interleukin 6 (IL-6) and transforming growth factor beta (TGF beta) concentrations were elevated, whereas % of renal tubular reabsorption of phosphate (%TRP) was decreased. The immunohistochemical results demonstrated the expression of PTHrP in atypical plasma cells. These data indicated that hypercalcemia complicating multiple myeloma causes an elevation of renal calcium reabsorption and an increase of bone resorption mediated by PTHrP action.


Subject(s)
Hypercalcemia/etiology , Multiple Myeloma/complications , Proteins/metabolism , Vitamin D/analogs & derivatives , Aged , Amino Acids/urine , Bone Marrow/pathology , Bone Resorption , Calcium/metabolism , Cyclic AMP/blood , Humans , Hypercalcemia/blood , Interleukin-6/blood , Kidney/metabolism , Male , Multiple Myeloma/pathology , Parathyroid Hormone/blood , Parathyroid Hormone-Related Protein , Transforming Growth Factor beta/blood , Vitamin D/blood
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