scholarly journals Myelofibrosis with myeloid metaplasia (MMM) - Idiopathic myelofibrosis - Agnogenic myeloid metaplasia

Author(s):  
F Cavazzini ◽  
A Cuneo
2002 ◽  
Vol 36 (9) ◽  
pp. 1380-1382 ◽  
Author(s):  
Giuseppe Famularo ◽  
Claudio De Simone

OBJECTIVE: To report a patient with lung cancer and idiopathic myelofibrosis with myeloid metaplasia who developed purpura and acute renal failure while receiving levofloxacin, and review the existing literature on quinolone nephrotoxicity. CASE SUMMARY: A 73-year-old white man, with a medical history of non-small-cell lung cancer and idiopathic myelofibrosis with myeloid metaplasia, was prescribed levofloxacin because of a lower urinary tract infection. Three days later, he presented with palpable purpura and erythematous skin lesions over the lower limbs and trunk, with a markedly reduced urinary output. Serum creatinine and urea nitrogen were 6.4 and 190 mg/dL, respectively. Levofloxacin was discontinued, and prednisone, furosemide, and intravenous fluids were given. The patient fully recovered over the ensuing 4 weeks. CONCLUSIONS: Nephrotoxicity associated with levofloxacin is uncommon. Allergic interstitial nephritis or vasculitis is believed to be the underlying pathologic process. Definitive diagnosis requires performance of renal biopsy, although this is not always feasible. In this case, a return of renal function to normal, with the disappearance of purpura following the discontinuation of levofloxacin and corticosteroid treatment, supports the presumptive diagnosis of a hypersensitivity reaction to levofloxacin.


2010 ◽  
Vol 54 (1) ◽  
pp. 151-153 ◽  
Author(s):  
Bijoy Patra ◽  
Anu Maheshwari ◽  
Jagdish Chandra ◽  
Satinder Aneja ◽  
Shilpi Agarwal ◽  
...  

1992 ◽  
Vol 147 (5) ◽  
pp. 1360-1362 ◽  
Author(s):  
Joseph E. Oesterling ◽  
Jerome P. Keating ◽  
Andrew J. Leroy ◽  
John D. Earle ◽  
George M. Farrow ◽  
...  

1999 ◽  
Vol 35 (3-4) ◽  
pp. 415-421 ◽  
Author(s):  
Niklas Zojer ◽  
Johannes Gobertus Meran ◽  
Michael Vesely ◽  
Helga Grüner ◽  
Jutta Ackermann ◽  
...  

1997 ◽  
Vol 21 (2) ◽  
pp. 125-131 ◽  
Author(s):  
Süleyman Özen ◽  
Burhan Ferhanoğlu ◽  
Mustafa Şenocak ◽  
Nükhet Tüzüner

1997 ◽  
Vol 34 (4) ◽  
pp. 341-345 ◽  
Author(s):  
K. N. M. Khan ◽  
A. C. Logan ◽  
E. M. Blomquist

Idiopathic myelofibrosis (IMF), or agnogenic myeloid metaplasia, was diagnosed in a sexually mature male marmoset { Callithrix jacchus) based on the results of hematology and histopathologic evaluation of the bone marrow. The hematologic changes included pancytopenia, leukoerythroblastosis, anisocytosis, poikilocytosis, and giant platelets. Histopathologic evaluation of the bone marrow showed marked widespread fibrosis replacing hematopoietic cells and the presence of atypical megakaryocytes. In addition, slight multifocal osteolysis with an increase in serum alkaline phosphatase activity was observed. We believe this is the first report of IMF in a nonhuman primate species.


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