Ds. David et al., VISCERAL VARICELLA-ZOSTER AFTER BONE-MARROW TRANSPLANTATION - REPORT OF A CASE SERIES AND REVIEW OF THE LITERATURE, The American journal of gastroenterology, 93(5), 1998, pp. 810-813
Objectives: Infection with varicella-zoster virus after bone marrow tr
ansplantation (BMT) is a common cause of morbidity and mortality. Visc
eral involvement with varicella-zoster mag be incorrectly ascribed to
graft-versus-host disease, resulting in delayed diagnosis and misguide
d therapy. Methods: A 4-yr retrospective chart review was performed to
determine the presenting symptoms and clinical outcome of visceral va
ricella-zoster virus infection in BMT recipients. Results: Ten BMT rec
ipients who subsequently developed visceral varicella-zoster virus inf
ection were identified. The mean age at diagnosis was 40 yr (range 27-
56 yr). Primary hematological malignancies were leukemia (N = 7), myel
odysplasia (N = 2), and myelofibrosis (N = 1). Bone marrow transplants
in affected patients were autologous (N = 2), related allogeneic (N =
5), or matched unrelated allogeneic (N = 3). The mean time interval f
rom BMT to symptomatic visceral varicella-zoster virus infection was 1
53 days (range 60-280 days). Presenting symptoms included abdominal pa
in in all patients, nausea (60%), fever > 38 degrees C (60%), vomiting
(50%), pneumonitis (50%), skin rash (40%), and diarrhea (30%). All pa
tients had moderately or profoundly elevated aminotransferases and mos
t had elevated pancreatic enzymes (80%). The mean time interval from t
he development of abdominal pain to the characteristic skin rash and t
hen diagnosis was 6 and 7 days, respectively (range 3-10 and 4-14 days
). Active graft-versus-host disease had previously been documented in
five of the eight allogeneic BMT recipients. Immunosuppressive medicat
ions were increased at the onset of the abdominal pain in seven of the
se eight patients for suspected exacerbation of graft-versus-host dise
ase. After recognition of varicella infection, antiviral therapy was p
romptly initiated; despite this, mortality was still 50%. Conclusions:
Visceral involvement with varicella-zoster virus infection can occur
as a late complication after both allogeneic and autologous BMT. In th
ese cases, symptoms of severe abdominal pain with associated nausea, v
omiting, and diarrhea and elevated liver and pancreatic enzymes preced
ed the vesicular skin eruption and were confused with graft-versus-hos
t disease. With the increasing application of high-dose chemotherapy f
ollowed by stem cell rescue for both hematological and solid tumors, c
linicians should be aware of this potentially treatable and often leth
al complication. (C) 1998 by Am. Cell. of Gastroenterology.