1.A case of Waldenström's macroglobulinemia treated using clarithromycin and prednisolone.
Masashi OHE ; Satoshi HASHINO ; Haruki SHIDA ; Tetsuya HORITA ; Mitsuru SUGIURA
Translational and Clinical Pharmacology 2017;25(3):134-137
We report a case of Waldenström's macroglobulinemia (WM) treated using clarithromycin (CAM) and prednisolone (PSL). An 84-year-old woman was admitted to our hospital for bleeding after a tooth extraction and hematuria. Computed tomography showed multiple ill-defined nodules in the omentum (omental cake). Although the cause of the omental cake remained unclear, the patient was diagnosed with WM, based on the detection of M-protein of immunoglobulin (Ig) M in serum and lymphoplasmacytes in bone marrow. The bleeding tendency in the patient may have been due to acquired hemophilia and/or hyper IgM-induced platelet dysfunction. The patient was treated using CAM (800 mg/day) and PSL (10 mg/day). As a result, IgM levels gradually decreased. Because the omental cake contracted along with improvement in IgM, it was thought to be lymphoplasmacytic lymphoma-like lymphoma. This case shows that treatment using CAM and PSL may be effective in some cases of WM.
Aged, 80 and over
;
Blood Platelets
;
Bone Marrow
;
Clarithromycin*
;
Female
;
Hematuria
;
Hemophilia A
;
Hemorrhage
;
Humans
;
Immunoglobulin M
;
Immunoglobulins
;
Lymphoma
;
Omentum
;
Prednisolone*
;
Tooth Extraction
;
Waldenstrom Macroglobulinemia*
2.A case of adult-onset Still's disease accompanied by pseudo-gray platelet syndrome.
Sumiyo MIYAKAWA ; Masashi OHE ; Haruki SHIDA ; Tetsuya HORITA ; Ken FURUYA ; Satoshi HASHINO
Blood Research 2017;52(3):231-233
No abstract available.
Blood Platelets*
;
Still's Disease, Adult-Onset*
3.Successful additional clarithromycin and tacrolimus treatment for hypereosinophilia associated with eosinophilic granulomatosis with polyangiitis
Masashi OHE ; Haruki SHIDA ; Tetsuya HORITA ; Ken FURUYA
Translational and Clinical Pharmacology 2018;26(2):60-63
A 41-year-old man suffering from eosinophilic granulomatosis with polyangiitis (EPGA), diagnosed at another clinic on the basis of American College of Rheumatology Criteria, with a history of bronchial asthma, eosinophilia, mononeuritis multiplex, and non-fixed pulmonary infiltrates, was admitted to our department for further treatment. The patient complained of chest pain that started recently. An echocardiogram identified myocardial thickening and decreased wall motion, based on which the patient was diagnosed as having EPGA with myocarditis. The patient was successfully treated using glucocorticoids, such as methyl prednisolone (PSL) and PSL in combination with cyclophosphamide (CPM). However, CPM administration was discontinued afterwards because of the risk of bone marrow toxicity, the increased eosinophilic count (EOC) that we considered as an index of disease activity. Subsequently, the patient received additional clarithromycin (CAM) and tacrolimus (TAC) treatment considering their immunomodulatory effects. As a result, the EOC decreased and the PSL dosage could be reduced. This case shows that additional CAM and TAC treatment may be beneficial in some cases of EPGA.
Adult
;
Asthma
;
Bone Marrow
;
Chest Pain
;
Clarithromycin
;
Cyclophosphamide
;
Eosinophilia
;
Eosinophils
;
Glucocorticoids
;
Granulomatosis with Polyangiitis
;
Humans
;
Mononeuropathies
;
Myocarditis
;
Prednisolone
;
Rheumatology
;
Tacrolimus
4.A case of follicular lymphoma accompanied with chylous ascites
Masashi OHE ; Masaru BABA ; Haruki SHIDA ; Ken FURUYA ; Katsuhisa KOGAWA
Blood Research 2019;54(3):163-163
No abstract available.
Chylous Ascites
;
Lymphoma, Follicular
5.Methotrexate-induced myelodysplasia mimicking myelodysplastic syndrome.
Yuuki KAWASE ; Masashi OHE ; Haruki SHIDA ; Tetsuya HORITA ; Ken FURUYA ; Satoshi HASHINO
Blood Research 2018;53(4):268-268
No abstract available.
Myelodysplastic Syndromes*