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Typical CT and MRI signs of hepatic epithelioid hemangioendothelioma

  • Authors:
    • Lu Gan
    • Ruiping Chang
    • Hualan Jin
    • Li Yang
  • View Affiliations

  • Published online on: January 26, 2016     https://doi.org/10.3892/ol.2016.4149
  • Pages: 1699-1706
  • Copyright: © Gan et al. This is an open access article distributed under the terms of Creative Commons Attribution License.

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Abstract

To investigate the typical magnetic resonance imaging (MRI) and computed tomography (CT) features of hepatic epithelioid hemangioendothelioma (HEH), the CT and MRI findings of 14 histopathologically confirmed cases of HEH were retrospectively analyzed. Non‑contrast and dynamic contrast‑enhanced scans were conducted in all cases. A total of 229 lesions were detected in the 14 cases. All cases were classified as one of three types: (i) Solitary nodular type (1 case, 7%); (ii) multifocal nodular type (11 cases, 79%); or (iii) diffuse type (2 cases, 14%). The diameter of the lesions ranged from 5 to 105 mm. For the first two types (solitary and multifocal nodular types), the CT findings included low density lesions with clear margins on non‑contrast scans, centripetal enhancement in arterial phase, and homogeneous enhancement in the portal venous and delay phases. The findings of non‑contrast MRI scans for these two types included low signal intensity on T1‑weighted images, heterogeneous high signal intensity on T2‑weighted images, and heterogeneous high signal intensity on diffusion‑weighted images. The lesions were predominantly located in submarginal areas. On contrast‑enhanced MRI, the findings for the first two types included peripheral ring‑like enhancement with a central low signal intensity (ʻblack target‑like’ sign) and a central enhanced core surrounded by a low signal intensity halo (ʻwhite target‑like’ sign). The findings for the third HEH type (diffuse type) on CT and MRI scans included low density or heterogeneous signal intensity lesions involving regions of part or the whole liver, coalescent lesions (ʻstrip‑like’ sign), and gradual enhancement along central vessels (ʻlollipop’ sign). Collectively, these findings indicate that the ʻwhite target‑like’ sign, ʻblack target‑like’ sign, ʻlollipop’ sign and ʻstrip‑like’ sign, in addition to capsular contraction and submarginal location, on CT and MRI imaging may have implications for the diagnosis of HEH. Furthermore, a variety of MRI sequences may provide additional information for the differential diagnosis of HEH.

Introduction

Hepatic epithelioid hemangioendothelioma (HEH) is a rare vascular tumor of endothelial origin with low- to intermediate-grade malignancy (1). HEH has a prevalence of 1 per 100,000 population (2). HEH may present as a solitary liver nodule or, more frequently, as multifocal liver nodules. Previous studies have revealed that HEH tends to coalesce into diffuse lesions in the late stages of the disease (3). Conventional treatments of HEH include surgical resection or liver transplantation. Previously, certain novel systemic drugs have been used in the treatment of HEH, including thalidomide and sorafenib (4,5). The prognosis for patients with HEH is considered much more favorable compared with that of other hepatic malignancies, with a 5-year survival rate of 43–55% (6).

Previously, HEH was frequently misdiagnosed as metastasis or, more rarely, as primary tumor of the liver, based on imaging and pathology (7). Pathological studies have indicated that myxoid, hyaloplasm and fiber compositions are present in the central part of HEH, which determine the appearance of the computed tomography (CT) and magnetic resonance imaging (MRI) scans and the enhancement patterns of the tumor (6,8). The peripheral region of the lesion, which is rich in tumor cells, demonstrates rim enhancement on the arterial phase, while the central part, which is rich in fiber composition, demonstrated delayed enhancement (9). Similar enhancement patterns have frequently been identified in cholangiocarcinoma (10). In addition, the fibrous contraction in the central region of the lesion caused the adjacent capsular contraction (3). The myxoid and hyaloplasm composition in the central region of HEH demonstrates no enhancement and the peripheral region demonstrates rim enhancement, termed the ‘black target sign’ or ‘bulls eye sign’, which may be frequently identified in metastatic tumors and hepatic abscesses (6).

Clinical presentation and history may be useful for the differential diagnosis of HEH, metastatic tumors and abscesses. The peripheral regions of certain hemangiosarcomas and atypical hemangiomas often demonstrate progressive enhancement, while the central necrosis or cystic regions demonstrate no enhancement (11). Differentiating HEH from the aforementioned tumors is challenging. At present, with the development and popularity of CT and MRI techniques, increasing numbers of characteristics associated with HEH have been extracted from CT and MRI images, including the ‘target sign’ and ‘lollipop sign’ (12). In addition, apparent diffusion coefficient (ADC) maps may be useful in revealing the malignant potential of the tumor (13). The final diagnosis of HEH depends on the pathology.

Thus, it is important to increase awareness of the imaging characteristics of HEH. In the current study, the CT and MRI findings of 14 cases of histopathologically confirmed HEH were retrospectively evaluated.

Materials and methods

Patients

Data from 14 cases of HEH, treated between 2010 and 2014 in the Chinese People's Liberation Army General Hospital (Beijing, China), were retrospectively collected. Informed consent from the patients was not required for this retrospective study as patient privacy was maintained. The diagnoses of 2 cases were determined by surgery, and 12 cases were confirmed by needle biopsy, with hematoxylin and eosin and immunohistochemical staining (BenchMark; Ventana Medical Systems, Inc., Tucson, AZ, USA). The immunohistochemical assessment was positive for cluster of differentiation 34 (CD34) and factor VIII-related antigen (12). The male:female ratio was 1:1, and the mean age of the patients was 43.5 years (range, 24–70 years). The percentage of asymptomatic cases was 50% (7 cases), whilst 21% (3 cases) presented with right upper quadrant pain, 28.5% (4 cases) presented with weight loss, and 7.1% (1 case) presented with jaundice and 7.1% (1 case) with fever. Only 1 case had a history of lung cancer resection. In 1 case, the level of carcinoembryonic antigen (CEA) was increased slightly (6.14 µg/l; normal range, 0.1–5 µg/l). The level of carbohydrate antigen 125 (CA125) was also increased in 1 case (63 U/ml; normal range: <5 units/ml).

Scan protocol

Non-contrast and two-phase dynamic contrast-enhancement CT scans were performed in 7 cases using a Siemens Sensation Cardiac 64 CT scanner (Siemens AG, Munich, Germany). In addition, 9 patients were examined by MRI (Signa Excite HD 1.5T; GE Healthcare Life Sciences, Shanghai, China). Patients were imaged in the supine position with a surface phased-array coil. For the complete evaluation of liver lesions, breath-hold transverse T2-weighted fast spin-echo sequences were initially performed, followed by transverse T1-weighted dual-echo in-phase and out-phase sequences, with a 5-mm slice thickness and 1-mm interspace. Three-dimensional fat-saturated T1-weighted dynamic contrast-enhanced sequences were performed during suspended respiration. Gadopentetate-dimeglumine (Gd-DTPA; 0.1 mmol/kg; GE Healthcare Life Sciences) was injected intravenously at a rate of 2 ml/sec by a power injector. Dynamic contrast-enhanced MRI was performed in the transverse plane with a 3-mm slice thickness and no interspace at baseline (pre-contrast), followed by the hepatic arterial-dominant (20–25 sec), portal venous (30–35 sec) and delay (300–360 sec) phases after contrast injection. Before dynamic contrast-enhanced imaging, transverse respiratory-triggered diffusion-weighted single-shot echo-planar imaging sequence was performed with tri-directional diffusion gradients by using two b-values of 0 and 800 sec/mm2.

Image analysis

All images were analyzed separately by two radiologists. Two reviewers analyzed all images with regard to the following aspects: Number, location and size of lesions; morphological features; intensity; and characteristics of dynamic contrast-enhanced images. By consensus through a joint review of the recorded images, each case was finally classified as one of the following types: (i) Solitary nodular type, a solitary lesion that has a diameter of <30 mm; (ii) multifocal type, multifocal lesions that may be separated from one another; or (iii) diffuse type, coalescent multifocal or diffuse lesions that have no clear margins between each other.

Results

Solitary nodular type

In 1 case, a solitary, low-density nodular lesion with an irregular shape was observed on non-contrast CT imaging, with slightly progressive enhancement on contrast-enhanced imaging (Fig. 1).

Multifocal nodular type
Number, size and distribution of lesions

Multifocal lesions were detected in 11 cases: 46 lesions were detected by CT in 4 cases, and 178 lesions were detected by MRI in 7 cases. In 4 cases (28.5%), the lesions were located in the right lobe of the liver, whilst in 1 case (7%) lesions were in the left lobe, and 6 cases (43%) involved the whole liver. The lesions were predominantly located in submarginal areas of the liver. Coalescent lesions were detected in a number of cases. The hepatic or portal veins were involved in 6 cases (42%). The diameters of the lesions ranged from 5 to 105 mm.

Patterns of lesion signal intensity

The lesions exhibited low density with clear margins on CT non-contrast imaging, and slight centripetal enhancement from the arterial to portal phases on contrast-enhanced CT imaging. On T1-weighted imaging (T1WI), the lesions exhibited low signal intensity. On T2-weighted imaging (T2WI), the lesions showed high signal intensity relative to the liver parenchyma, and the scattered or coalescent lesions, located in submarginal areas, showed a ‘white target-like’ sign or ‘strip-like’ sign; the two-layered ‘target-like’ appearance was formed by the high-signal intensity core and peripheral slightly hyperintense halo. On diffusion-weighted imaging (DWI), the lesions showed a high-signal intensity halo outside of the central slightly high-signal intensity core. ‘Target-like’ configurations were detected in 141 cases (60.5%) (Figs. 2 and 3). On dynamic contrast-enhanced MRI scans, the enhancement features varied with different blood supply patterns. In total, 160 lesions (70%) exhibited gradual peripheral ring-like enhancement patterns, with central low signal intensity in the arterial to portal venous and delay phases, and 51 cases (24%) showed peripheral ring-like enhancement patterns with central low signal intensity in arterial phase, and the enhanced lesions were surrounded by a thin hypointense ring in the portal venous or delay phases (‘black target-like’ sign) (Fig. 3). Liver capsular flattening or retraction was observed in 60 lesions (27%), and 1 case (4%) exhibited ‘strip-like’ coalescence of multifocal nodules (Fig. 3). Nodular enhancement along the central vessels (‘lollipop’ sign) was observed in 10 lesions (4%) (Fig. 4). Heterogeneous-intensity masses surrounded by several nodules were present in 5 cases (36%); the masses exhibited peripheral nodular enhancement in the arterial phase and gradual homogeneous enhancement in portal venous phase. The transient abnormal perfusion of the peripheral liver parenchyma was visualized in the arterial phase and disappeared in portal venous phase (Fig. 4).

Diffuse type

Diffuse lesions throughout the whole liver were observed in 2 cases. The CT features included diffuse low-density lesions with minimal residual areas of normal liver parenchyma, in addition to nodular or irregular enhancement in the arterial phase and gradual enhancement in portal venous phase. The MRI features included heterogeneous low signal intensity on T1WI and high signal intensity on T2WI, with patchy uniform signal intensity within the lesions. Nodules and masses coexisted in the 2 cases. Nodules exhibited ‘target-like’ signs on non-contrast imaging and heterogeneous enhancement on contrast-enhanced imaging, while masses showed ‘strip-like’ enhancement along central vessels in the arterial phase and gradual enhancement in the portal venous and delay phases. Stenosis or occlusion of the portal and hepatic veins were also detected (Fig. 5).

Other findings

Metastatic tumors in the lung, spleen, thoracic vertebra, ilium or thoracic wall were detected in 4 cases (28.5%), a liver abscess was observed in 1 case (7%), and ascites was present in 1 case (7%). The hepatic or portal veins were involved in 6 cases (42%).

Methods of definitive diagnosis

All cases were misdiagnosed prior to surgery or needle biopsy: 2 cases were diagnosed as malignant tumor of the liver, 4 cases were diagnosed as cholangiocellular carcinoma, 4 cases were diagnosed as metastatic tumors, 1 case was diagnosed as hepatic fibrosis and 2 hypovascular cases were undetermined.

Discussion

The present study investigated the CT and MRI characteristics of HEH. The findings revealed a number of typical CT and MRI signs associated with HEH, most notably the ‘white target-like’ sign on contrast-enhanced MRI.

HEH is a rare malignant tumor of vascular origin. It was described as being characterized by the presence of ‘epithelioid’ or ‘histiocytoid’ endothelial cells in 1982 by Weiss and Enzinger (14), who used the term ‘epithelioid hemangioendothelioma’ to designate these biologically ‘borderline’ neoplasms. HEH appears to have a clinical course between benign hemangioma and angiosarcoma. The World Health Organization classifies HEH as a malignant tumor (10). In the majority of patients, both lobes of the liver are involved, and lung, peritoneum, lymph nodes and bone are the most common sites of simultaneous extra-hepatic involvement (1,15). HEH predominantly occurs in adult females; the mean age of patients is ~41.7 years, and the female:male ratio is 1.6–2.0:1. The etiology of HEH remains unknown; however, it may be associated with oral contraceptive use, exposure to polyethylene, trauma or viral hepatitis (2,6,16).

In the current study, a total of 229 lesions were detected, most of which were located in the submarginal areas of the liver, and 56% of which had capsular flattening or retraction; this was lower than that reported by Miller et al (3) and Paolantonio et al (17), but similar to that reported by Zhao et al (18), in which capsular retraction was observed in 59.5% of HEH in Chinese patients. MRI has been demonstrated to have advantages over CT in the detection of submarginal and small size lesions. Certain studies indicated that submarginal nodular lesions may be an earlier form of HEH, as they later gradually transform into the diffuse type (3,19,20).

In the current study, HEH was classified into three types according to the number of lesions: Solitary nodule, multifocal nodule and diffuse types. The percentage of solitary nodular-type cases (7%) was markedly lower than that in previous reports (2,4). This may be due to the fact that the imaging features of the solitary nodular-type disease are relatively non-specific (21).

On the contrary, multifocal nodular and diffuse types had a more typical appearance on CT and MRI. On non-contrast CT scans, tumors appeared as low density lesions with clear margins. On T1WI, the lesions exhibited low signal intensity whilst, on non-contrast T2-weighted fat-suppressed imaging, the lesions exhibited heterogeneously high signal intensity relative to the adjacent normal liver parenchyma. On DWI, the lesions appeared with slightly high-signal intensity cores and a high-signal intensity halo; these two-layered ‘target-like’ configurations were detected in 141 lesions (60.5%).

On contrast-enhanced MRI, the enhancement features varied with different blood supply patterns. Multifocal lesions were classified into four categories according to different enhancement patterns: (i) Slightly irregular homogeneous enhancement; (ii) peripheral enhancement with central low signal intensity in the arterial phase, and enhanced lesions surrounded by a thin hypointense ring in the portal venous and delay phases (‘black target-like’ sign); (iii) nodular enhancement in the central part of the lesion in the arterial phase surrounded by ring-like enhancement in the portal venous and delay phases (‘white target-like’ sign); and (iv) peripheral nodular enhancement in the arterial phase and centripetal enhancement in the portal venous and delay phases, an enhancement pattern that is more commonly indicated in hemangioma.

In the current study, 79% of lesions exhibited a ‘target-like’ sign on T2WI, and 70% of lesions exhibited the ‘black target-like’ sign on contrast-enhancement scans. This was consistent with previous reports (9,2225). In the study by Fan et al (23), the HEH was revealed to possess slightly increased signal intensity with increased signal intensity centers on the T2-weighted image, and ‘ring-like’ peripheral enhancement on the post-contrast enhanced MRI. In the study by Chen et al (9), HEH presented as two types (the multifocal and diffuse types), and 96.4% of the two types presented as the ‘target sign’ with a progressive enhancement rim on the contrast-enhanced multiple-phase MRI. The study by Bruegel et al (24) indicated that HEH showed a ‘target-like’ sign on T2, DWI and ADC maps, and the lesions also showed a variable degree of peripheral rim enhancement Notably, the ‘white target-like’ sign on contrast-enhanced imaging had not previously been described; we hypothesize that this unique sign may have value with regard to the diagnosis of HEH. As the majority of cases were confirmed by needle biopsy, the relationship between the ‘white target-like’ sign and histopathological features remains unknown. As the core of the lesion had high signal intensity on T2WI and low signal intensity on contrast-enhanced T1WI, the ‘white target-like’ sign may correlate with central necrosis in the lesion. A thin, hypointense ring outside of a peripherally enhanced halo (‘black target-like’ sign) in the portal venous or delay phases may correlate to a layer of fibrous tissue between the lesion and the normal liver parenchyma (3). Certain previous studies have revealed that, during the hepatobiliary phase, the lesions may exhibit a contrast-enhanced core surrounded by a low-signal intensity halo; the central enhancement was indicated to be due to ‘entrapment’ of contrast agent in the central fibrous stroma, and the peripheral hypointense halo due to the lack of hepatobiliary enhancement in the peripheral tumor zone (17,21).

In the present study, a ‘lollipop’ sign was also observed, as reported by Alomari (12). The detection of the involvement of the portal and hepatic veins on the CT and MRI scans were satisfactorily consistent with the pathology, as the scans were able to detect all involved portal and hepatic veins that were proven by pathological methods. In a study by Makhlouf et al (6), calcification was detected in 20% of lesions; however, none was observed in the current study, probably due to the insensitivity to calcification of MRI (3,26,27). With regard to diffuse-type HEH, similar CT features to the present study were reported by Baron et al (28).

In the current study, one case was misdiagnosed as hepatic fibrosis with a sub-marginal ‘strip-like’ sign; this sign may indicate the coalescence of multifocal nodules. None of the 14 cases in the study were diagnosed correctly based on CT and MRI findings, as the imaging characteristics of HEH were not widely recognized at the time of diagnosis, particularly for the solitary nodular-type cases. It is difficult to distinguish solitary HEH from metastatic tumors or cholangiocellular carcinoma (6).

The clinical symptoms of HEH vary greatly, and the disease may be asymptomatic or present with non-specific symptoms. Typically, HEH is present for a long time before a definitive diagnosis is made (2). For example, in the present study, hepatic lesions were found in 1 patient ~4 years prior to a definitive diagnosis. In the present study, 7 cases (50%) had non-specific complaints, 3 cases (21%) had right upper quadrant pain, 3 cases (28.5%) had weight loss, 1 case (7%) had jaundice attributable to the tumors, 1 case (7%) had fever, and 1 case (7%) had nausea. This was consistent with previous reports (1,6). Makhlouf et al (6) collected 137 cases of HEH with nonspecific symptoms, including right upper quadrant pain or weight loss. In the study by Ishak et al (1), 12.5% of cases were asymptomatic. With regard to biochemical examinations, the concentrations of serum bilirubin, alkaline phosphatase and aspartate aminotransferase are typically significantly increased (2). In addition, the majority of cases are negative results for presence of tumor markers, and only a few cases exhibit slightly increased levels of CEA (26). In the present study, CEA levels were marginally increased in 1 case (6.14 µg/l), CA125 levels were increased in 1 case (63 U/ml), and tumor markers were negative in the other cases. Thus, the tumor markers most commonly used in clinical practice have no significant value for the diagnosis of HEH.

Histologically, HEH is composed of dendritic and epithelioid cells that often contain vacuoles representing intracellular lumina. Furthermore, at least one of the endothelial markers (factor VIII-related antigen, CD34 and/or CD31) is positively expressed (6,29). Microscopically, characteristic spindle- and oval-shaped cells with abundant eosinophilic cytoplasm are observed (30). Commonly, biopsy is able to confirm a diagnosis of HEH; however, an insufficient size of biopsy specimen may results in failure to diagnose to HEH, and laparoscopic liver biopsy is preferred in order to obtain adequate specimens for analysis (31). Fortunately, in the current study, definitive diagnosis could be made with needle biopsy in the majority of cases.

Management strategies for HEH include liver resection, liver transplantation, transcatheter arterial chemoembolization and palliative treatment (2,32). Recent studies have suggested that immediate treatment may not be the optimal strategy (33). HEH often follows an indolent course. In a previous study, there was no difference of 5-year survival in patients with unilateral or bilateral lesions, localized or metastatic disease, even with an initial treatment regimen of surgery (33) Therefore, the biological behavior of the tumor may be associated, in part, with its matrix, which may exhibit inflammation, dense sclerosis and calcification. Assessment of disease behavior may better stratify treatment options (33). For unresectable HEH, liver transplantation is the best option; studies have demonstrated that the long-term survival time is very good, and much better than in HCC patients (29). One study indicated that 62.5% of patients with HEH survived for over 5 years, and one patient succumbed 28 years subsequent to the initial diagnosis (1).

The limitations of the present study include its retrospective nature, the fact that it was conducted in a single center, and the small sample size. Further studies are required to identify more novel signs associated with HEH.

In conclusion, HEH is a rare tumor that may present certain typical imaging features, including the ‘white target-like’, ‘black target-like’, ‘lollipop’ and ‘strip-like’ signs, capsular contraction, submarginal distribution. These features may contribute significantly to the definitive diagnosis of HEH. Use of a variety of MRI sequences may provide more information for the differential diagnosis of HEH.

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Gan L, Chang R, Jin H and Yang L: Typical CT and MRI signs of hepatic epithelioid hemangioendothelioma. Oncol Lett 11: 1699-1706, 2016.
APA
Gan, L., Chang, R., Jin, H., & Yang, L. (2016). Typical CT and MRI signs of hepatic epithelioid hemangioendothelioma. Oncology Letters, 11, 1699-1706. https://doi.org/10.3892/ol.2016.4149
MLA
Gan, L., Chang, R., Jin, H., Yang, L."Typical CT and MRI signs of hepatic epithelioid hemangioendothelioma". Oncology Letters 11.3 (2016): 1699-1706.
Chicago
Gan, L., Chang, R., Jin, H., Yang, L."Typical CT and MRI signs of hepatic epithelioid hemangioendothelioma". Oncology Letters 11, no. 3 (2016): 1699-1706. https://doi.org/10.3892/ol.2016.4149