A 45-year-old man was a known case of lung chemical injury due to the exposure to the mustard gas in the war 20 years ago. Although he had lung injury following exposure to the mustard gas he remained free of any lung symptoms until recent years. He reported a 1-year history of non-productive cough. This cough was described as paroxysmal mostly during day time, unaccompanied by constitutional signs, such as fever. Although the patient’s cough persisted more than one year, the diagnosis of cough was not sought exactly during his prolonged period. He has been to numerous doctors for his conditions (COPD) but the medications were not effective. His appetite was good and denied any GI symptoms such as pain, diarrhea, constipation, bleeding, vomiting, nausea, melena, hematemesis etc. The patient’s coughing was noted to be vigorous in recent months and several chest X-rays couldn’t show any pathology in lung in past. Clinicians requested computed tomography (CT) scan of the chest which revealed lung metastasic lesions (diffuse small nodular lesions) and a large liver mass in few images of chest CT. The patient was referred to our GI clinic for more evaluation. His physical examination was unremarkable except for multiple nevus (brown papules and macula with regular borders and pigment) which were seen on his back.
Laboratory data showed: WBC: 10300/mm
3 (Neutrophil: 60%, Lymphocyte: 22%, Monocyte: 1%, Eosinophil: 17%), Hb: 10.9 g/dlit, PLT: 223,000/mm
3 , ESR 1
st hr: 90mm, ESR 2
nd hr: 104mm, AST: 17IU/L, ALT: 29 IU/L, ALP: 417 IU/L (up to 306), T Bili: 0.3 g/dlit, D Bili: 0.1 g/dlit, PT: 15, INR: 1.3, PTT: 45, T protein: 7.4 g/dlit, Albumin: 3.6 g/dlit, Urea: 30, Cr: 0.9 ng/ml, CEA: 2.3 ng/ml, AFP: 1.3, CA 19-9:9 U/ml and LDH: 328 IU/L. Anti HCV, HBS Ag, and HBS Ab: negative. Peripheral blood smear just showed hypochromia, anisocytosis, and microcytosis in red blood cells. Serology of hydatid cyst was negative. Then, we requested abdominal and pelvic CT scans (
Figures 1 and
2).
An ill-defined hypodense mass is evident in segment three of left hepatic lobe (thin arrow), mildly extending to caudate lobe (curved arrow), which shows mild homogeneous contrast enhancement in delayed phase. There is also proximal dilatation of intrahepatic bile ducts at subcapsular region of left lobe due to mass effect (thick arrow) (
Figure 2). There are two peripherally located hypodense mass lesions in subcapsular portion of right hepatic lobe (segment 6) without significant enhancement in this phase. One of them shows central punctate calcification (thick arrow). There is also an enlarged lymph node at aortocaval region (curved arrow).
Radiologist reported that liver size was normal and its density was homogenous. There was a large heterogeneous and mild enhancing mass with lobular margin, measuring about 120×85 mm in the left lobe of liver which almost occupied the left lobe entirely. Large vascular of the left lobe was encased and displaced by the mass, but these were not seen within IVC (inferior vena cava) and portal vein thrombosis. At least four similar and smaller mass within 6
th segment of liver lobe were depicted. Conglomerated lymph adenopathies were seen in the celiac axis and peripancreatic region. Gall bladder, intra and extra hepatic biliary tree were normal and ascities was not seen. We performed needle biopsy of the liver under ultrasonography guide. Pathologist reported EHE diagnosis with immnohistology. (
Figure 3) He was referred to an oncologist for chemotherapy due to metastatic lesions.