- Case report
- Open Access
- Open Peer Review
Inflammatory pseudotumor of the liver: a case report and review of the literature
© Ntinas et al; licensee BioMed Central Ltd. 2011
- Received: 9 July 2010
- Accepted: 21 May 2011
- Published: 21 May 2011
Inflammatory pseudotumor of the liver represents a fairly uncommon pathology. Although it is a benign tumor, the correct diagnosis can be missed.
We report the case of a 55-year-old Caucasian man, who presented with a one-month history of abdominal pain and weight loss. He was diagnosed with a primary liver tumor by computed tomography and magnetic resonance imaging. Alpha-fetoprotein levels ranged within normal limits. A right posterior sectorectomy was performed. Histopathology revealed an inflammatory pseudotumor of the liver. Our patient remains in good condition one year later.
Although inflammatory pseudotumor of the liver is usually a benign process, controversy regarding its management still exists. With this case report we review the existing literature and consider hepatectomy as a safe treatment approach.
- Sclerosing Cholangitis
- Fibrous Histiocytoma
- Focal Liver Lesion
- Inflammatory Myofibroblastic Tumor
Inflammatory pseudotumors (IPTs) are reactive conditions that occur in many organs. They have been reported in the lung, which is the most common site of occurrence, central nervous system, major salivary glands, kidney, liver, omentum, ovary, larynx, urinary bladder, breast, pancreas, spleen, lymph nodes, skin, soft tissues, orbit etc. . The first report of an hepatic IPT was published by Pack and Baker in 1953 . This entity has also been described as inflammatory myofibroblastic tumor, plasma cell granuloma, histiocytoma and fibroxanthoma. Someren classified inflammatory pseudotumors into three groups according to histology. The first of these is xanthogranuloma-type pseudotumors, the second is plasma cell granuloma-type pseudotumors and finally there are sclerosing pseudotumors . Macroscopically, the lesion may mimic a malignancy and may be single or multiple. Its dimensions may be up to 25 cm. Microscopically, IPT is characterized by spindle-shaped cells, myofibroblasts and mixed inflammatory cells (plasma cells, lymphocytes and, sporadically, histiocytes).
The literature survey to date indicates 130 publications with 289 cases of hepatic IPTs [4–6]. The prevalence of this condition, although low, is not irrelevant. In a retrospective analysis of 403 patients who underwent surgery for focal liver lesions, the incidence of IPTs was 0.7% . Published data report that out of 188 patients with IPT, 106 underwent liver resection and 76 were treated conservatively, 5 out of whom subsequently also had to undergo surgery because their initial medical treatment failed . Upon diagnosis, the proposed treatment of IPTs is rather conservative, administering either antibiotics or steroids . However, occasional reports advocated the use of more radical treatment, that is to say, its resection [1, 4].
The etiology and pathogenesis of IPTs remain unknown . Frequently an infectious agent is implicated. In many reports, the responsible microorganisms found include Bacteroides caccae, Actinomyces, Klebsiella, Escherichia coli, Gram-positive cocci and β-hemolytic streptococcus. This could explain why, in some cases, the decrease or even resolution of IPTs occurs after treatment with antibiotics. However, in other reports, no causative microorganisms have been identified, which could imply the association of IPTs with hepato-pancreato-biliary autoimmune diseases, such as IgG4 sclerosing cholangitis . Based on this, many reports suggest therapeutic management (tumor resolution) with steroid administration. Differentiating between IPTs and other focal hepatic lesions remains a major problem, despite progress in imaging technology. Unfortunately, IPTs may mimic malignant lesions (lymphoma, malignant fibrous histiocytoma, hepatocellular carcinoma, metastatic tumor, etc.) and granulomatous lesions (tuberculosis and sarcoidosis) . The CT-scan usually reveals lesions with variable contrast enhancement. IPTs may present with hypovascular character because of fibrosis and also show a delayed enhancement, similar to metastatic liver tumors and cholangio-carcinomas . The MRI may produce low signal intensity (hypointense) on T1-weighted images with moderate to high signal intensity (hyperintense) on T2 sequence [4, 7]. Because MRI provides additional information about hepatic lesion characteristics, it is often used in our institute in the metastatic work-up.
In general, it is difficult to distinguish IPTs from malignant tumors by radiographic studies. Literature shows that in some (individual) cases a percutaneous tumor biopsy provided the correct diagnosis. These patients were treated with antibiotics and/or corticosteroids with complete resolution of the lesion; however, some of these lesions have recurred . In contrast, there have been numerous studies reported where hepatic resection was employed, mainly due to the pre-operative malignant radiographic appearance of the tumor, and incidentally resected IPTs never recurred .
A further problem suggested in the literature, besides recurrence, is the potential malignant transformation of IPTs some years after hepatectomy. It has even been reported that some patients died of this disease. In particular, the authors report that these patients developed non-Hodgkin lymphoma, hepatic sarcoma and recurrence of IPTs with multiple hepatic masses and extension to the thorax some years later [11, 12].
Regarding the current case, liver biopsy was not used as a diagnostic tool due to the strong suspicion of the lesion's malignant character, provided by the imaging findings. While liver biopsy has an undoubted role in the investigation and management of liver metastases of unknown origin, it plays a doubtful and probably dangerous role in patients with a solitary hepatic mass with high probability of malignancy . Needle tract seeding has been reported to occur in 5.1% of patients with hepatocellular carcinoma (HCC), who underwent percutaneous needle biopsy . Hemorrhage, with mortality rates less than or equal to 1 in 10,000 biopsies in experienced centers, is another possible, although rare, complication . Furthermore, for the planning of a liver surgical intervention, biopsy of the tumor is not necessary.
A fairly uncommon clinical entity was presented. IPTs are often difficult to distinguish from hepatic malignant tumors. The safety of hepatectomy of non-cirrhotic patients has increased over the past 20 years, with mortality converging to 0%, therefore surgical resection should be considered as treatment of choice in such cases . This approach is preferable because it not only minimizes the risk of a biopsy-related complication (dissemination in cases of malignancy), but it also abolishes the possibility of IPT recurrence.
Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
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