Abstract
First reported in 1976, hepatic angiomyolipoma (HAML) is a rare mesenchymal liver tumor occurring mostly in middle-aged women. Diagnosis of the liver mass is often incidental on abdominal imaging due to the frequent absence of specific symptoms. Nearly 10% of HAMLs are associated with tuberous sclerosis complex. HAML contains variable proportions of blood vessels, smooth muscle cells and adipose tissue, which renders radiological diagnosis hazardous. Cells express positivity for HMB-45 and actin, thus these tumors are integrated into the group of perivascular epithelioid cell tumors. Typically, a HAML appears on magnetic resonance imaging (or computed tomography scan) as a hypervascular solid tumor with fatty areas and with washout, and can easily be misdiagnosed as other liver tumors, particularly hepatocellular carcinoma. The therapeutic strategy is not clearly defined, but surgical resection is indicated for symptomatic patients, for tumors showing an aggressive pattern (i.e., changes in size on imaging or high proliferation activity and atypical epithelioid pattern on liver biopsy), for large (> 5 cm) biopsy-proven HAML, and if doubts remain on imaging or histology. Conservative management may be justified in other conditions, since most cases follow a benign clinical course. In summary, the correct diagnosis of HAML is challenging on imaging and relies mainly on pathological findings.
Keywords: Angiomyolipoma, Liver, Tuberous sclerosis complex, Imaging, Pathology, Potentially malignant
Core Tip: Hepatic angiomyolipoma (HAML) is a rare, but not exceptional, mesenchymal liver tumor. HAML contains variable proportions of blood vessels, smooth muscle cells and adipose tissue, which renders its radiological diagnosis challenging. In most cases, this tumor follows a benign clinical course but more aggressive behavior may complicate management, which remains poorly codified. This review presents the main demographic and histological characteristics of HAML, summarizes reported cases of HAML with spontaneous rupture and aggressive behavior, and finally proposes a pragmatic algorithm for the management of HAML based on the most recent knowledge.
INTRODUCTION
Angiomyolipoma (AML) is a solid mesenchymal tumor, mainly described in the kidney, and belongs to the group of perivascular epithelioid cell tumors (PEComas)[1]. Hepatic localization of AML, described for the first time in 1976[2], is rare, since only around 600 cases were reported after an exhaustive search of the literature up to the year 2017[3]. Hepatic AML (HAML) poses a veritable diagnostic challenge in radiological terms, especially when fat content is low, because this type of tumor may appear as a hypervascular tumor associated with a washout phase that mimics other, more common hypervascular hepatic tumors, such as hepatocellular carcinoma[4-7]. The natural course of HAML is mostly benign, although several cases have been reported to exhibit aggressive behavior with metastasis or recurrence after surgery[8-24], or spontaneous rupture[8,25-33]. These rare but dramatic observations unavoidably compound the complexity of managing patients with HAML. Due to its difficult radiological diagnosis, its potentially aggressive behavior, and its poorly codified management, we aimed to analyze the recent literature regarding this rare, but not exceptional liver tumor, and to provide a pragmatic algorithm for its management according to the most recent knowledge.
PATIENT CHARACTERISTICS
HAML is a tumor usually occurring in a non-cirrhotic liver, and mainly affects middle-aged women. A retrospective analysis of the literature carried out up to 2016 identified 292 patients with one or more HAML, and most of them (nearly 74%) were women, with a median age ranging between 24 years and 53 years across studies[3]. HAML mainly locates in the right liver (60% of cases[7]), is unique in 84% of cases, and median size ranges from 2 cm to 12.7 cm[3,34]. This type of tumor is often detected incidentally during medical check-ups (42% to 72% of cases) since most subjects are asymptomatic[3,34,35]. Symptoms revealing HAML may include abdominal pain or discomfort, bloating, weight loss or, more rarely, discovery of an abdominal mass on palpation[35]. A few cases of spontaneous rupture of HAML have been reported (Table 1)[8,25-33]. Tumor size (≥ 4 cm) and pregnancy are two recognized conditions favoring rupture of renal AML[36,37], but the small number of reported cases of HAML rupture precludes identification of predictors of rupture in the liver. In the ten cases reported in Table 1, tumor size was usually large, between 5 cm and 12 cm (except for one case due to an inflammatory variant of HAML with a subcapsular location[32]), and there was no age preference (mean age: 48 years; range: 22 years to 77 years). All patients underwent emergent or delayed resection of the tumor, sometimes preceded by preoperative embolization. Routine laboratory tests (including liver tests) are usually normal, as are serum tumor markers (alpha-fetoprotein, carcinoembryonic antigen and carbohydrate antigen 19-9[38].
Table 1.
Ref.
|
Sex
|
Age, yr
|
Symptoms
|
Abdominal radiological findings
|
Treatment
|
Outcomes
|
Huber et al[25] 1996 | F | 22 | Hemorrhagic shock with clinical symptoms of acute abdomen | CT scan: multiple tumors of the liver (the largest in segment III measured 8 cm) and both kidneys and a splenic lesion with a diameter of 4 cm | Surgical resection of segments II and III | Postoperative course was uneventful. Discharge from hospital 12 d later |
Guidi et al[26] 1997 | M | 74 | Sudden onset of upper-quadrant pain | CT scan: liver tumor of 10 cm × 8 cm in the segments I and V and another small mass of 4 cm × 3 cm in segment IV. Fluid was present in the upper abdominal compartments | Surgical resection of the hemorrhagic hepatic mass | Postoperative course was uneventful. Discharge from hospital 8 d later |
Tsui et al[27] 1999 | F | 41 | Acute rupture of a subcapsular tumor | 9 cm | Surgical resection | Patient in healthy condition 4 yr after surgery |
Zhou et al[28] 2008 | ND | ND | Hemorrhagic shock | Ultrasonography showed a 5-cm "cavernous hemangioma" in the right hepatic lobe | Emergency laparotomy for hemostasis | No tumor recurrence or metastasis was found during follow-up of 2-3 yr |
Ding et al[8] 2011 | F | 56 | ND | A rupture of the tumor measuring 6 cm × 6 cm in segment VI was confirmed by emergent laparotomy | Liver suture followed by segmentectomy | No serious morbidity in the postoperative course |
Occhionorelli et al[29] 2013 | F | 25 | Sudden onset of abdominal upper-quadrant pain and hypotension, after two recent syncopal episodes | CT scan showed a hepatic tumor in the left lobe (8.6 cm × 7.2 cm) with suspected peritoneal blood leakage | Hemorrhage initially managed by manual compression, followed by deep and pro-coagulant tissue adhesives. After 48 hours, the patient underwent left-liver lobectomy | Postoperative course was uneventful. Discharge from hospital 9 d later |
Aoki et al[30] 2014 | F | 70 | Sudden onset of back pain on the right side | CT scan: hepatic tumor in segment VII measuring 7 cm in diameter accompanied by subcapsular hematoma with extravasation | Transcatheter arterial embolization. Right hepatic lobectomy was carried out 39 d later | Five days after surgery, she had thrombi in the left popliteal vein and the left pulmonary artery. Insertion of an IVC filter which was removed due to sepsis. She was discharged 24 d after surgery. There was no recurrence 42 mo following surgery |
Tajima et al[31] 2014 | M | 38 | Upper abdominal pain | CT scan showed a tumor measuring 10.5 cm × 9.5 cm × 7 cm in the posterior segment of the right hepatic lobe that had ruptured into the space between the liver and the diaphragm | Transcatheter arterial embolization was performed. The patient developed fever and the hematoma surrounding the liver was drained. No infection was confirmed but right lobectomy was performed | ND |
Kai et al[32] 2015 | F | 77 | Sudden abdominal pain and transient loss of consciousness | CT scan: hemoperitoneum with subcapsular hematoma at the left lobe and a hepatic nodule measuring 2.3 cm in diameter in segment II | Conservative initial treatment with periodic imaging studies. Transcatheter arterial chemoembolization was performed because a diagnosis of HCC was suggested. Surgical resection (laparoscopic left lateral segmentectomy) was performed 4 mo later | Postoperative course was uneventful. Discharge from hospital 7 d later No signs of recurrence at 3.5 yr after surgery |
Kim et al[33] 2017 | M | 31 | Sudden onset severe abdominal pain in the right upper quadrant area | CT scan: Mass of approximately 12 cm in the right hepatic lobe with hemorrhage along the perihepatic space | Emergent angiography with embolization.Hepatic resection was performed 15 d later | Postoperative course was uneventful |
F: Female; M: Male. ND: Not determined; CT: Computed tomography; HCC: Hepatocellular carcinoma; IVC: Inferior vena cava.
The association between tuberous sclerosis complex (TSC) and renal AML, first described in 1911[39], is observed in 50% of cases, while the association between TSC and HAML is only observed in 5% to 15% of cases[3,40]. TSC is an autosomal dominant genetic disorder with a birth incidence of 1:6000[41], although sporadic cases due to de novo mutation are the most frequent presentation in the absence of a family history. TSC results from a mutation of TSC1 or TSC2, which code for hamartin and tuberin, respectively[42]. These proteins are critical regulators of cell growth and proliferation, potentially through their upstream modulator, mammalian target of rapamycin (mTOR). Loss of function or dysfunction of either protein results in the development of hamartomas in numerous organ systems, including the brain, kidneys, heart and liver[43]. In patients with TSC, HAML is frequently associated with renal AML. A recent retrospective study showed that among 25 patients with HAML, 88% also had renal AML, and TSC2 patients had a higher frequency of HAML compared to TSC1 patients (18% vs 5%; P = 0.037)[42]. In contrast to previous reports, the predominance of female gender observed in patients with HAML but no TSC was not observed in patients with the TSC-HAML association[42,44].
IMMUNOHISTOLOGICAL CHARACTERISTICS OF HAML
Histological examination is the gold standard for HAML diagnosis, since diagnosis by imaging is difficult. Of note, even histological analysis of liver biopsy was shown to misdiagnose HAML in about 15% of cases in a recent multicenter study[34]. The World Health Organization defines PEComas as “mesenchymal tumors containing distinctive perivascular epithelioid cells”. AML, which belongs to the PEComa group, is composed of adipose tissue, smooth muscle and vessels with dystrophic walls (Figure 1). The histological and immunohistochemical characteristics class HAML in the group of PEComas, an entity that brings together tumors of different histology, but with a common immunohistochemical signature, namely co-expression of melanocytic and muscle markers (see below)[1,40,45]. The PEComa family includes AML, clear cell “sugar” tumor of the lung, lymphangioleiomyomatosis (LAM), and a variety of unusual visceral, intra-abdominal, and soft tissue/bone tumors, described under the term “clear cell myomelanocytic tumor of the falciform ligament/Ligamentum teres”[46]. There is a strong association between AML and TSC, and between LAM and TSC[47], although the link is less marked for other members of the PEComa family[46].
Perivascular epithelioid cells are characterized by their perivascular location, often with a radial arrangement of cells around vessels. Typically, these cells are mostly epithelioid when they are just around the vessels, whereas spindle cells resembling smooth muscle are seen further away from the vessels. In the liver, the aspect is most often only epithelioid without spindle cells. Adipose cells are usually found distant from the blood vessels. Wide variation is seen in the relative proportion of epithelioid, spindle, and lipid-distended cells. Depending on the relative proportion of these different tissues, there are, on the one hand, conventional AMLs with a predominance of lipomatous or myomatous cells or vessels, and, on the other hand, epithelioid AMLs containing at least 10% epithelioid cells[48]. Mixed and myomatous AMLs are the most frequent (respectively 36% and 42% of the 151 HAML cases with informative data)[3]. Another subtype of HAML, namely inflammatory HAML, has also been recognized, although only 14 cases have been reported in the English-language literature[49]. Overall, this tumor is characterized by inflammatory infiltration exceeding 50% of tumor area, and the main types of inflammatory cells are lymphocytes (100%), plasma cells (93%) and histiocytes (71%)[49].
Macroscopically, HAML is well circumscribed, unencapsulated, smooth and brownish in color; however, the existence of hemorrhage or intra-tumor necrosis can change its appearance. On microscopic examination, cells typically have clear or slightly eosinophilic cytoplasms, small, central, round or oval nuclei, with a small nucleolus. "Atypical" AML presents cytological atypia, a multinucleated nucleus, focal necrosis and an increase in the number of mitoses[48].
By immunohistochemistry, these tumors are positive for both melanocytic markers (HBM-45 and melan-A are the more sensitive markers) and smooth muscle markers (actin and/or desmin) with variable extent of staining[46,50]. HBM-45 is the most specific marker of AML[38]. Actin non-immunoreactivity does not exclude a tumor from the PEComa group[51]. Classically, AML does not express epithelial markers (like cytokeratin), S100 protein or alpha-fetoprotein[52]. Estrogen and progesterone receptors are frequently positive in classic renal AML but are only rarely positive in extrarenal PEComas, including HAML, suggesting the absence of the role of sex hormones in the pathogenesis and growth of HAML, despite a clear predominance in women[45,53].
There are numerous possible differential diagnoses of PEComas depending on the location and the predominant tissue composing the tumor. Given their uniform expression of melanocytic markers, PEComas may be confused with both conventional melanoma and clear cell sarcoma, but these latter typically have strong expression of S100 protein, and do not stain with smooth muscle actin. Due to its preferential abdominal location, the presence of epithelioid and spindle cells, and the occasional positive KIT (CD117) staining in HAML, the diagnosis of gastrointestinal stromal tumor is sometimes discussed. Depending on the size of the contingent of epithelioid cells, spindle-shaped cells or adipocytes, AML can also be confused with carcinoma, smooth muscle neoplasm or adipocytic tumor[45,54].
PROGNOSIS
The scarcity of PEComas precludes the identification of robust criteria to discriminate benign AML from other tumors with more aggressive behavior. The first description of a likely “malignant” HAML is recent[55], and although the authors do not clearly indicate the malignant nature of this tumor, the reported characteristics (i.e., large size, cytological atypia and presence of necrosis) and the tumor-related death of the patient are robust arguments in favor of a “malignant” case. From a series of 24 PEComas of the soft tissue and gynecologic tract (not including AML) with a median follow-up of 30 mo (range: 10-84), Folpe et al[46] observed 3 local recurrences and 5 distant metastases (8/24, 33% of cases), 2 deaths (8%), 4 patients (17%) alive with metastatic or unresectable local disease, and 18 patients (75%) alive with no evidence of disease. A combined analysis of these 24 cases plus 45 other reported cases in the literature with sufficient available follow-up information identified the following variables associated with an increased risk of recurrence or metastasis: tumor size greater than 5 cm, infiltrative growth pattern, high nuclear grade, necrosis, and mitotic activity > 1/50 high power field. Consequently, these authors developed a provisional classification of PEComas with increasing aggressive potential (Table 2). Cases of HAML with aggressive behavior are reported in Table 3[8-24]. Regarding HAML, it is mainly the epithelioid type that confers a risk of aggressive behavior[34]. In the review published in 2017, the mortality rate associated with HAML was 0.8%[3].
Table 2.
Classification
|
Criteria
|
Benign | No worrisome features: (1) Tumor size < 5 cm; (2) No infiltration; (3) Non-high nuclear grade and cellularity; (4) Mitotic activity ≤ 1/50 HPF; (5) No necrosis; and (6) No vascular invasion |
Uncertain malignant potential | Tumor with: (1) Pleomorphism/multinucleated giant cells only; or (2) Size > 5 cm only |
Aggressive behavior | Two or more worrisome features: (1) Size > 5 cm; (2) Peripheral infiltration; (3) High nuclear grade and cellularity; (4) Mitotic activity > 1/50 HPF; (5) Ischemic tumor necrosis for large tumor; and (6) Vascular invasion |
According to the WHO classification of tumors[1] | As with GISTs, the main predictors of a risk of metastatic behavior are marked nuclear atypia, diffuse pleomorphism and mitotic activity of more than 1 mitosis per 1 mm² |
GIST: Gastrointestinal stromal tumor; HPF: High-power field.
Table 3.
Ref.
|
Sex
|
Age, yr
|
Size
|
Types
|
Treatment
|
Duration of follow-up
|
Outcome
|
Croquet et al[9] 2000 | F | 16 | 19 cm × 12 cm × 8 cm | Epithelioid | SR | 6 yr | Recurrence in the liver, associated with renal angiomyolipoma |
Dalle et al[10] 2000 | F | 70 | 15 cm | Epithelioid | SR | 5 mo | Recurrence in the liver with a lesion measuring 15 cm and presence of multiple metastases in the liver |
Flemming et al[11] 2000 | F | 51 | 2 nodules: 0.5 cm and 15 cm | Epithelioid | SR | 3 yr | Recurrence in the right hepatic lobe and presence of multiple metastases |
McKinney et al[12] 2005 | F | 14 | 11 cm × 7 cm × 8 cm | NS | SR, interferon α | 1 yr | Recurrence with a hepatic lesion measuring 9 cm × 6 cm × 14 cm, appearance of lymph nodes and hepatic metastases. Death after disease progression |
Parfitt et al[13] 2007 | F | 60 | 14 cm × 11 cm | Epithelioid | SR | 9 yr | Recurrence in the liver and appearance of metastases in the trapezius muscle, the left lung and the tail of the pancreas |
Yang et al[14] 2007 | F | 37 | 13 cm × 9 cm × 9 cm | Classic | SR | 14 mo | Recurrence in the right hepatic lobe 6 months after SR, appearance of pulmonary metastases 11 mo after SR and death occurred at 14 mo |
Deng et al[15] 2008 | M | 30 | 18 cm × 14 cm | Classic | SR, Chemotherapy | 3 yr and 4 mo | Recurrence with a hepatic lesion measuring 11 cm and metastases in pancreatic tail and portal vein thrombosis 3 yr after SR. Chemotherapy was initiated but 4 mo later pulmonary metastases appeared. Death occurred after disease progression |
Nguyen et al[16] 2008 | F | 43 | 11 cm × 7.5 cm × 7.5 cm | Classic | SR | 6 mo | Recurrence in the liver 6 mo after SR, together with metastases in the peritoneum, omentum, stomach and spleen. Death after disease progression |
Xu et al[17] 2009 | F | 33 | 2 nodules: 1 cm and 6 cm | Epithelioid | SR | 1 yr | Recurrence in the left hepatic lobe |
Zeng et al[18] 2010 | NS | NS | 6 cm | NS | SR | 9 yr | Recurrence in the right hepatic lobe with a lesion measuring 6 cm |
Butte et al[19] 2011 | F;M | 54; 41 | NS; 9 cm | NS; Epithelioid | SR; SR | 53 mo; 41 mo | Recurrence in the liver 53 mo after SR; Occurrence of pulmonary and retroperitoneal metastases 41 mo after SR |
Hu et al[20] 2011 | F | NS | NS | NS | SR | 14 mo | Appearance of local and distant metastases 6 mo after SR. Death occurred 14 mo after SR |
Ding et al[8] 2011 | F | 31 | 8 cm × 8 cm | NS | SR | 7 yr | Recurrence in the right hepatic lobe 6 yr after SR and death occurred one year later |
Wang et al[21] 2015 | F | 37 | 7 cm × 9 cm | Classic | SR | 3 yr | Recurrence of two hepatic nodules in the right lobe (13 cm × 12 cm and 2.3 cm × 1.8 cm) 3 yr after SR. Arterial chemoembolization was performed, followed by liver transplantation |
Fukuda et al[22] 2016 | M | 58 | 6.3 cm | Epithelioid | SR | 9 yr | Metastases occurred in the right lung 7 yr after SR and were treated by pneumonectomy. No recurrence was observed after 2 yr of follow-up |
Marcuzzi et al[23] 2018 | F | 47 | 3.8 cm × 4.6 cm × 4.7 cm+ 2 hepatic lesions measuring 6 mm and 5 mm | Epithelioid | SR | 8 yr and 8 mo | CT scan was performed 6 yr and 4 mo after the initial presentation: the hepatic lesion had grown in size to an estimated 10.9 cm × 9.7 cm × 11.2 cm and the adjacent lesions had grown to 1.9 cm and 2.4 cm with a new lesion on the kidney of 4.6 cm × 5.1 cm. 16 mo later, MRI showed an increase in size of the hepatic lesion (12 cm × 11 cm), and kidney lesion (6.2 cm × 5.6 cm). SR performed 2 mo later. 6 mo after SR, recurrence in the resection line and in the hepatic segment II |
Yan et al[24] 2018 | NS | NS | 15 cm | Epithelioid | SR | 9 yr | Recurrence in the liver 9 yr after SR with invasion of the inferior vena cava and diaphragm, and appearance of pulmonary metastases |
F: Female; M: Male; NS: Not specified; SR: Surgical resection; CT: Computed tomography; MRI: Magnetic resonance imaging.
Imaging findings
The imaging features of HAML vary greatly depending on the highly variable proportion of fat, smooth muscle and vascular elements. Diagnosis can be challenging, and depends mainly on the amount of fat present, which is the key to HAML diagnosis. On ultrasound, the lesion is usually well circumscribed, hyperechoic or mixed echoic and after injection of ultrasound contrast, presents rapid enhancement in the arterial phase compared to the adjacent liver. In the portal and delayed phase, HAML can display either hypo, iso or hyperenhancement[4]. Computed tomography (CT) shows a hypodense tumor with fatty areas within the lesion (density around -50 HU). Classically, this solid tumor is hypervascular (Figure 2) with wash-out in the portal and late portal phase [CT or magnetic resonance imaging (MRI)]. HAML with few or no vessels on histologic examination show persistent portal and late-phase enhancement, whereas HAML with richly vascularized tissue is more likely to show wash-out[5]. The tumor signal on MRI is hyperintense in T2 weighted sequences and variable in T1 weighted sequences. MRI is the most sensitive imaging technique to detect liver fat using in-phase and opposed-phase T1 gradient echo sequences. The drop-out signal within a liver lesion on the opposed-phase sequences indicates the presence of fat within the lesion (Figure 3A and B). The imaging features on MRI after injection of contrast medium are similar to those observed on CT scan. When using a hepatocyte specific agent (gadoxetic acid or gadobenate dimeglumine), the lesion shows a hyposignal in the hepatobiliary phase (Figure 4).
Data regarding HAML evaluation using fluorine-18-fluorodeoxyglucose positron emission tomography (18F-FDG-PET) are limited. FDG uptake in HAML is variable and the value of 18F-FDG-PET for diagnosing or managing this type of tumor is unclear[56].
Given the imaging characteristics of HAML (hypervascular lesion with a fat component in a healthy liver and with frequent wash-out), differential diagnoses are benign hepatocytic tumors (steatotic or telangiectasia adenoma, fat focal nodular hyperplasia) and malignant hepatocytic tumors (mainly hepatocellular carcinoma). When the diagnosis is challenging, especially with hepatocellular carcinoma, the absence of a capsule and the visualization of a drainage vein are two useful radiological features that can be helpful for HAML diagnosis when they are present[6].
MANAGEMENT OF HAML
Due to its rarity, the diagnosis of HAML on imaging (and even histological examination[34]) is difficult. Consequently, the clinical management of HAML patients should take place in expert centers for a multidisciplinary work-up involving radiologists, pathologists and hepatologists. Obtaining a liver biopsy is strongly advised to better balance the risk of surgery (resection of centrohepatic tumor will be at higher risk, for instance) against the risk of tumor-related complications. Thus, in the presence of asymptomatic HAML, without cytological atypia on biopsy, but at high risk of complicated resection, regular radiological monitoring will be preferred[34].
Analysis of the literature shows that the majority of patients are treated with surgical resection (84% and 76% of patients in two large case series[3,34]). For other patients, regular radiological monitoring is justified by the uncertainty surrounding the risk of HAML progression. Although the risk of tumor recurrence after resection or metastases has rarely been described, the identification of radiological and especially histological factors predicting an unfavorable course (Table 1) is essential for a collegial therapeutic decision. Furthermore, patient compliance with regular radiological monitoring will also be an important argument in decision-making[3,35].
The optimal radiological follow-up is not well defined, but the first radiological evaluation may take place at one year, since HAMLs were described to increase by only 0.77 cm per year in a series of 29 patients followed radiologically[3], and radiological progression affected only 6 of the 29 patients (20%). Later, radiological monitoring could be performed twice a year[3], but the frequency will depend on the magnitude of tumor progression during the first years of monitoring. Evidently, persistent tumor progression on successive imaging will require a surgical approach. Surgical resection is therefore recommended when there is uncertainty regarding the histological nature of the lesion after liver biopsy, tumor progression on imaging, tumor-related symptoms, and when the tumor exceeds 5 cm[34,38]. The recurrence rate after surgical resection was 2.4% (6 of 246 patients in the series reported by Klompenhouwer et al[3]). The local or distant post-resection recurrence rate is 10% in the case of epithelioid-type HAML[52].
Liver transplantation (LT) has sometimes been erroneously performed for a suspected diagnosis of cholangiocarcinoma or hemangiosarcoma mimicking a hepatocellular carcinoma[3,34]. These flawed diagnoses further underline the interest of systematic liver biopsy as well as radiological and anatomopathological expertise. Since the first reported case of LT for HAML in 2010[57], other exceptional cases have been added[21,58]. LT was performed as a last resort treatment for unresectable HAML due to excessive size or a significant number of hepatic tumors.
Other therapeutic alternatives have been reported, such as radiofrequency ablation, arterial embolization or the use of sirolimus[35,42]. mTOR inhibitors, which include sirolimus and everolimus, are immunosuppressive molecules used in transplantation, and which also have antiproliferative properties. In a multicenter, double-blind, placebo-controlled, phase 3 trial (EXIST-2), 118 patients with at least one renal AML larger than 3 cm associated with a definite TSC diagnosis or sporadic LAM were randomized to receive oral everolimus 10 mg/d (n = 79, mean dosage: 8.6 mg/d, median duration: 38 wk) or placebo (n = 39). The trial showed a beneficial effect of everolimus in reducing the size of AML (response rate: 42% vs 0% in the placebo group; P < 0.0001). Response was evaluated as a composite endpoint including a reduction ≥ 50% of the AML volume[59].
The favorable outcomes reported in the EXIST-2 trial led to an open label extension undertaken by the same authors. This study demonstrated a pronounced benefit of everolimus for the patients who continued on this drug. The response rate improved from 42% in the primary analysis (median exposure 8.7 mo)[59] to 54% (median exposure 28.9 mo), and the long-term use of everolimus appeared safe[60].
The pooled analysis of two randomized trials[59,61] comparing 109 and 53 patients with renal AML treated respectively with everolimus and placebo for 6 mo confirmed the efficacy of everolimus in reducing tumor volume by 50% or more (risk ratio = 24.69; P = 0.001)[62]. Everolimus is currently indicated for the treatment of adult patients with renal AML and TSC not requiring immediate surgery. Some patients with HAML associated with TSC have been treated with sirolimus, which also proved efficacious in reducing tumor volume[54]. The role of mTOR inhibitors for patients with HAML remains undefined, but these molecules could be used, as for the kidney, in a palliative context. The long-term safety profile is consistent with that previously reported and no new safety issues have raised concern[60].
In a retrospective Chinese series (2009-2016) of 92 patients diagnosed with histologically proven HAML measuring between 2 cm and 5 cm, ultrasonography-guided radiofrequency ablation after liver biopsy was used in 22/92 patients. No tumor recurrence was reported, but the duration of follow-up was not indicated[35]. Radiofrequency ablation can therefore advantageously compete with surgery when HAML is relatively small (< 5 cm), and when the location in the liver or the patient’s comorbidities are not amenable to safe hepatic surgery.
Arterial embolization[33] is sometimes necessary in the presence of hemorrhagic HAML. There are only eight reported cases of HAML presenting as spontaneous rupture and hemorrhage; the median size of these tumors was 8.5 cm (range: 2.5 cm to 12.5 cm) and three of them were treated with arterial embolization followed by liver resection enabling formal diagnosis of HAML. The main differential diagnosis of hemorrhagic liver tumor in a non-cirrhotic liver is adenoma, which is outside the scope of this review. Therapeutic arterial embolization was used in three other patients with histologically proven HAML (size: 11, 12 and 17 cm) in a retrospective American series[19], and no progression was observed after an average follow-up of 12.7 mo (range, 1-36 mo). The risk of spontaneous hemorrhage seems to be lower for HAML than for kidney AML, which are usually supplied by a single vessel and associated with aneurysms[19]. We propose a decisional algorithm for the management of HAML (Figure 5).
CONCLUSION
HAML is a rare but not exceptional tumor, and usually has a benign course. However, this tumor may display more aggressive behavior with recurrence or metastasis, although there are no robust histological or radiological characteristics to predict the natural course of this type of tumor. Radiological diagnosis is often hazardous due to the variable proportions of the tissues that comprise HAML. Therefore, histological analysis of the tumor and multidisciplinary consultation, whenever possible in an expert center, are essential for optimal care of these patients.
Footnotes
Conflict-of-interest statement: No conflicts of interest exist.
Manuscript source: Unsolicited manuscript
Peer-review started: October 27, 2020
First decision: December 18, 2020
Article in press: March 18, 2021
Specialty type: Gastroenterology and hepatology
Country/Territory of origin: France
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P-Reviewer: Alshami A, Lan C S-Editor: Gao CC L-Editor: Webster JR P-Editor: Liu JH
Contributor Information
Paul Calame, Department of Radiology, Jean Minjoz University Hospital, Besançon 25030, France.
Gaëlle Tyrode, Department of Hepatology, Jean Minjoz University Hospital, Besançon 25030, France.
Delphine Weil Verhoeven, Department of Hepatology, Jean Minjoz University Hospital, Besançon 25030, France.
Sophie Félix, Department of Pathology, Jean Minjoz University Hospital, Besançon 25000, France.
Anne Julia Klompenhouwer, Department of Surgery, Erasmus University Medical Center, Rotterdam PO Box 2040, The Netherlands.
Vincent Di Martino, Department of Hepatology, Jean Minjoz University Hospital, Besançon 25030, France.
Eric Delabrousse, Department of Radiology, Jean Minjoz University Hospital, Besançon 25030, France.
Thierry Thévenot, Department of Hepatology, Jean Minjoz University Hospital, Besançon 25030, France. tthevenot@chu-besancon.fr.
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