Zobrazeno 1 - 10
of 16
pro vyhledávání: '"S J Vukelja"'
Autor:
J. Redmond, S. J. Vukelja, H. Auerbach, R. S. Charles, N. Dawson, T. Reid, R. Tenglin, D. Faragher, M. P. Richter, M. A. Samaha
Publikováno v:
Southern Medical Journal. 88:305-308
Bilateral synchronous testicular cancer is a rare occurrence usually associated with similar histologic findings in each testicle. We describe eight patients with bilateral synchronous testicular germ cell cancer, of whom four had dissimilar histolog
Autor:
Craig Smith, K A Konkol, K C Abbott, T J O'Rourke, M Ristic, C J Holland, C K McAllister, S J Vukelja
Publikováno v:
American Journal of Hematology. 38:230-234
A 67-year-old white man with human ehrlichiosis infection complicated by pancytopenia, hemophagocytic syndrome, disseminated intravascular coagulopathy and septic shock is presented. The patient had been on a three-week camping trip to California, Co
Publikováno v:
Annals of Hematology. 74:287-289
An unusual case of co-existing Gilbert's syndrome and hereditary spherocytosis is reported. Diagnostic strategies are presented, and the literature is reviewed for simultaneous presence of these disorders.
Publikováno v:
Cutis. 59(4)
A case of acute myelocytic leukemia of the FAB-M2 subtype in a patient who experienced pigmentary nail changes in conjunction with idarubicin therapy is presented. Although doxorubicin and daunorubicin have been reported to cause nail pigmentation ch
Publikováno v:
Medical and pediatric oncology. 27(3)
The authors present a case of radiation recall dermatitis occurring in a patient receiving paclitaxel shortly after completion of radiation therapy. A brief review of previously reported taxane-induced radiation recall reactions is provided.
Publikováno v:
American journal of hematology. 51(2)
Essential thrombocythemia (ET) is an uncommon myeloproliferative disorder, which is thought to develop from a multipotent stem cell. Like other myeloproliferative diseases, ET is associated with an increased risk of development of acute leukemia (AL)
Publikováno v:
Cancer. 74(11)
Lymphomatoid papulosis (LyP) is an uncommon disorder characterized by recurrent papulonodular cutaneous lesions that last from 4 to 5 weeks and often heal with hypopigmented or hyperpigmented scarring. Prognosis is varied, 10%-20% of patients have as
Publikováno v:
Bone marrow transplantation. 12(3)
Autologous BMT performed in a 57-year-old woman with relapsed large cell lymphoma was complicated by two consecutive episodes of diffuse alveolar hemorrhage (DAH). The second episode occurred immediately after infusion of autologous BM. DAH is an inc
Publikováno v:
Cutis. 52(2)
A nineteen-year-old woman whose Hodgkin's disease had relapsed experienced acral erythema in association with a asymptomatic pericardial friction rub following autologous bone marrow transplantation. An echocardiogram revealed a large pericardial and
Publikováno v:
Journal of the American Academy of Dermatology. 25(5 Pt 2)
A variety of cutaneous reactions have been reported with the use of systemic 5-fluorouracil. Our patient had serpentine hyperpigmented streaks appearing 5 days after bolus infusion of 5-fluorouracil. The patient also had other skin eruptions, that is