Varicella zoster-associated gastric ulcers, hepatitis and pancreatitis in an immunocompromised patient

Inhaltsübersicht

A 62-year-old man presented with severe, continuous abdominal pain to a general hospital. His previous medical history revealed autologous stem cell transplantation for multiple myeloma 3 months before admission. This was complicated by bronchiolitis obliterans organizing pneumonia (BOOP) for which treatment was instituted with 25 mg prednisone per day. An abdominal computed tomography (CT) scan showed evidence of acute pancreatitis and despite appropriate treatment intense abdominal pain persisted. During the following days he developed a skin rash, which was interpreted as drug-induced, and a generalized seizure. After 7 days he was referred to our hospital. Physical examination revealed an ill man in great pain. On clinical examination he had a maculovesicular rash on the face, trunk, and abdomen ([Fig. 1]). Laboratory investigation showed elevated serum aspartate aminotransferase of 1038 U/l (normal 0 – 36 U/l), alanine aminotransferase 848 U/l (normal 0 – 40 U/l), amylase 158 U/l (normal 0 – 99 U/l), C-reactive protein 57 mg/l (normal 0 – 9 mg/l), and leukocyte count 3.2 × 10⁹/L (normal, 3.5 – 10.0 × 10⁹/L). A chest X-ray showed diffuse infiltrative pulmonary abnormalities. Upper gastrointestinal endoscopy revealed multiple well-demarcated superficial erosions with a white patchy surface in the esophagus ([Fig. 2]). In the fundus, corpus, and antrum of the stomach, multiple ulcers with central necrosis were present, ranging from 5 mm to 10 mm in diameter ([Fig. 3]). The abdominal pain, skin rash, and the multiple ulcerations in the esophagus and stomach raised clinical suspicion of varicella zoster virus (VZV) infection. Polymerase chain reaction (PCR) revealed VZV genome in serum, as well as in skin and gastric biopsies.

Fig. 1 Maculovesicular skin rash on the trunk.

Fig. 2 Multiple well-demarcated superficial erosions with a white patchy surface in the distal esophagus.

Fig. 3 Ulcers with central necrosis along the greater curvature of the corpus of the stomach.

VZV is an unsuspected cause of severe acute abdominal pain and patients may present with hepatitis, pancreatitis, and gastroesophageal mucositis. Moreover, VZV infection is the most common viral disease after bone marrow transplantation, occurring in 17 – 50 % of patients, with a median interval of 3 – 6 months [1] [2]. In the majority of cases, cutaneous manifestations precede those of abdominal organ dissemination, making early diagnosis more likely [2]. Timely diagnosis and prompt treatment may diminish mortality, which ranges from 9 % to 55 % [1] [2] [3]. In most cases, latent VZV is reactivated from the dorsal root ganglia, which share the afferent sympathetic fibers that supply the liver, pancreas, gastrointestinal mucosa, and lungs [3]. Since posterior sensory nerve roots contain fibers from both skin and abdominal viscera, these organs are potential candidates to be affected [3]. In our patient, all of these organs were affected and after treatment with intravenous aciclovir 10 mg/kg/8 h, the abdominal pain as well as the cutaneous and pulmonary abnormalities disappeared and serum amylase and transaminase levels normalized.

In conclusion, the combination of multiple gastric ulcers, pancreatitis, hepatitis, and a skin rash should raise the possibility of disseminated VZV infection, especially following bone marrow transplantation.

Endoscopy_UCTN_Code_CCL_1AB_2AD_3AC

Competing interests: None

References

• 1 Takatoku M, Muroi K, Kawano-Yamamoto C et al. Involvement of the esophagus and stomach as a first manifestation of varicella zoster virus infection after allogeneic bone marrow transplantation.  Intern Med. 2004;  43 861-864
• 2 Rivera-Vaquerizo P A, Gomez-Garrido J, Vicente-Gutierrez M et al. Varicella zoster gastritis 3 years after bone marrow transplantation for treatment of acute leukemia.  Gastrointest Endosc. 2001;  53 809-810
• 3 Stratman E. Visceral zoster as the presenting feature of disseminated herpes zoster.  J Am Acad Dermatol. 2002;  46 771-774