Orbital alveolar soft part sarcoma: A report of 8 cases and review of the literature

Abstract

Alveolar soft part sarcoma (ASPS) is a rare soft tissue neoplasm. The incidence of orbital involvement is the highest in ASPS arising in the head and neck region. However, limited information is available regarding its clinical characteristics. The present study presents the clinical manifestations, imaging findings, pathological features, treatment strategies and prognosis records of 8 cases of orbital ASPS over the last 15 years in a single hospital, along with a review of the literature. Included were 3 male and 5 female patients, with the median age at presentation being 9.5 years. The mean average largest tumour diameter was 3.6 cm. A total of 5 patients underwent surgical excision of the tumour, with 2 undergoing orbital exenteration and 1 undergoing partial orbital exenteration. In total, 6 patients received postoperative radiotherapy and 2 received chemotherapy. Upon follow-up, 6 patients were doing well with no evidence of recurrence or metastasis. Local recurrence developed in 2 patients, of whom 1 succumbed following withdrawal from treatment. According to the present series and the cases mentioned in the literature, orbital alveolar soft part sarcoma has characteristics distinct from those of alveolar soft part sarcoma which arises in other locations. Orbital alveolar soft part sarcoma presents itself in a younger population with a shorter course of disease, smaller tumour size, improved prognosis, a marked association with the extraocular muscles and with the Ki-67 proliferation index possibly associated with prognosis of the disease.

Introduction

Alveolar soft part sarcoma (ASPS) is a rare form of soft tissue neoplasm that accounts for between 0.5 and 0.9% of all soft tissue sarcomas, and between 1 and 15% of malignant tumours in adults and children, respectively (1). ASPS may occur at any age, with a peak incidence in the third decade of life. ASPS is usually identified in the extremities in adults, and the head and neck region in children, particularly the orbit and tongue. However, it is rare for primary ASPS lesions to form in the orbit. In the present study, the clinical manifestations, imaging results, pathological features, treatment strategies and prognosis of 8 cases of orbital ASPS over the last 15 years were reviewed. Domestic and foreign literature regarding ASPS was also reviewed for further comprehension of this rare type of tumour.

Materials and methods

Ethics statement

The present retrospective study was approved by the Medical Ethics Committee of the General Hospital of Chinese People's Armed Police Forces (Beijing, China) and conducted in compliance with the tenets of The Declaration of Helsinki. All patients or their parents provided written informed consent.

Patients

Patients with orbital ASPS who were treated over the last 15 years (from January 2000 to April 2015) at the General Hospital of Chinese People's Armed Police Forces were considered in the present study (n=8). A comprehensive retrospective review was performed to evaluate the characteristics of this type of sarcoma. Information regarding the clinical course, including clinical manifestations and treatment, was collected from the patients' medical records. Computed tomography (CT) and magnetic resonance imaging (MRI) results were acquired from the database at the General Hospital of Chinese People's Armed Police Forces. Outcome information was obtained from follow-up data and phone calls to the patients or their parents.

Haematoxylin and eosin (H&E)-stained slides, periodic acid-Schiff (PAS)-stained slides and immunohistochemical slides were available in all cases. The diagnosis of ASPS was confirmed by the review of these slides by experienced pathologists at the General Hospital of Chinese People's Armed Police Forces.

A review of the English literature based on a PubMed search spanning 1963 to 2013 and a review of the Chinese literature based on a China Knowledge National Infrastructure search spanning from 1981 to 2014 were performed, and all cases of orbital ASPS with detailed data were included. Cases were excluded if they were duplicated or their information was too generalized.

Results

Clinical data and ophthalmological examination

From a total of 8 patients, 3 were male and 5 were female, with age at presentation ranging between 2 and 51 years (median, 9.5 years). Patients <20 years of age made up 75.0% (n=6) of the sample, of which 5 were <10 years of age (62.5%). The duration of symptoms ranged between 9 days and 1 month. The tumour was located in the right orbit in 3 cases and the left orbit in 5 cases. Clinical manifestations were mainly proptosis and abnormal position of the eye (Fig. 1). Certain individuals also exhibited accompanying eyelid swelling, blepharoptosis, headache, ophthalmodynia, impaired vision, diplopia and subconjunctival vasodilatation. Detailed data are presented in Table I.

Figure 1.

Clinical image of case 5 demonstrating non-axial proptosis of the left eye with downward and rightward displacement of the globe.

Table I.

Clinical features of patients with orbital alveolar soft part sarcoma.

Patient	Age, years/sex	Eye affected	Course of disease	Clinical features	Tumour location	Tumour size, cm	Management	Follow-up
1	19/M	Right	1 mh	Proptosis, diplopia, ophthalmalgia, anorthopia, ocular motility restriction, conjunctival congestion, papilloedema	Medial part of the orbit, adhering to medial rectus muscle, extending to apex	2.5×1.5×1.5	S+R	6 mh, no Rec or M, lost
2	51/F	Right	1 mh	Proptosis, ophthalmalgia, anorthopia, lid swelling, palpable mass, papilloedema	Medial optic nerve, indistinguishable from medial rectus muscle	3.5×3.5×1.2	S+E+R	Lost
3	2/F	Right	1 mh	Proptosis, ophthalmalgia, anorthopia	Inside inferior rectus muscle throughout its length to apex	5.0×3.6×0.8	S	Gave up therapy, 2 mh Rec, 1 yr succumbed
4	6/M	Left	15 days	Proptosis, ptosis, lid swelling, ocular motility restriction	Inside superior rectus muscle	2.0×1.5×1.2	S+R	61 mh, no Rec or M
5	2/M	Left	1 mh	Proptosis, tearing, anorthopia, ocular motility restriction	Between superior rectus muscle and levator palpebrae superioris muscle	2.0×2.0×2.0	S+R	49 mh, no Rec or M
6	9/F	Left	9 days	Proptosis, lid swelling, ocular motility restriction	Inside medial rectus muscle	4.5×3.0×1.0	E+R+C	13 mh, no Rec or M
7	10/F	Left	20 days	Proptosis, lid swelling, diplopia, pain, vision impaired, anorthopia, ocular motility restriction, papilloedema	Inferolateral, indistinguishable from inferior and lateral rectus muscle and optic nerve	4.5×3.0×1.5	B+E	13 mh, no Rec or M
8	32/F	Left	1 mh	Vision impaired, diplopia, proptosis, ophthalmalgia	Indistinguishable from lateral rectus muscle	5.0×3.0×2.0	S+R+C	3 mh, no Rec or M

B, biopsy; S, surgical excision; E, exenteration; R, radiotherapy; C, chemotherapy; Rec, recurrence; M, metastasis; mh, months; yr, years.

Table II summarizes the cases of orbital ASPS reported in the literature listed on PubMed (1–22), excluding this series. There were 55 cases (33 female and 22 male patients) between 1963 and 2014, with a median age at diagnosis of 12 years (ranging between 10 months and 69 years). The lesion was located in the right orbit in 19 cases, the left orbit in 22 cases and the location of the mass was not provided in 14 cases. The median tumour size was 2.95 cm in the largest diameter. Table III summarizes the cases reported in the Chinese literature from 1981 to 2014 (23–36). There were 9 female and 10 male patients, totalling 19 cases, with a median age at diagnosis of 11 years (range, 2–53 years). The lesion was located in the right orbit in 7 cases and in the left orbit in 12 cases. The median tumour size was 2.45 cm. When summing up the data in Tables I–III, there were 82 patients with orbital ASPS (47 female and 35 male patients), with a median age of 12 years at diagnosis. The median tumour size was 2.85 cm. There was a slight female predilection (female/male ratio, 1.34:1) in orbital ASPS when compared with ASPS arising in other locations.

Table II.

Reported cases in PubMed of orbital alveolar soft part sarcoma.

No.	Author	Country	Number of cases	Age (median)	Sex	Eye affected	Tumour location	Tumour size, cm	Management	Follow-up	(Refs.)
1	Mulay et al, 2014	India	9	1–31 (6) yr	2 M, 7 F	NM	Intraconal, close to optic nerve: 1; association with and indistinct from extraocular muscles: 8	NM	7: S+R; 2: S+R+C	6–126 mh (median 43 mh)/no Rec or M	(2)
				12 yr	F	L	Surrounding optic nerve	3.9×2.5×2.3	B+E	2 mh/no Rec/M
2	Kim et al, 2013	USA	2	22 yr	M	L	Involving temporalis muscle	4.5	B+S+R+E+C	7 mh/local Rec, 2 mh/Rec involving anterior cranial fossa, M to lungs and liver	(3)
3	Majumdar et al, 2013	India	1	25 yr	M	R	Abutting superior rectus muscle	NM	S	6 mh/no Rec or M	(4)
4	Rekhi et al, 2012	India	2	19 yr	M	NM	NM	3.0×3.0×2.0	S	39 mh/M to lungs, alive	(5)
				31 yr	M	NM	NM	NM	S	NM
5	Rose et al, 2011	Kenya	1	5 yr	M	L	Replace superior rectus muscle throughout its length	NM	S	1 mh/no Rec or M	(1)
				15 mh	M	L	Antero-inferior orbit	2.9×1.8	NM	NM
6	Alkatan et al, 2010	Saudi Arabia	2	6 yr	F	R	Superior orbit, associated with superior and medial rectus muscles	NM	NM	NM	(6)
				3 yr	F	R	NM	1×1×1.5	S	3 mh/Rec
7	Pang et al, 2008	China	3	10 yr	F	R	NM	1.5×1×0.8	S	6 mh/Rec	(7)
				11 yr	F	R	NM	7×6×4	S	Lost
8	Morris et al, 2005	USA	1	45 yr	F	L	Retrobulbar, medially	2.2×2.0×0.8	S	3 mh/no Rec or M	(8)
				15 yr	M	NM	Lower eyelid	2.0	S+R+C	16 yr/no Rec or M
9	Kanhere et al, 2005	India	2	14 yr	F	NM	Orbit, no details	3.0	E+R	1 yr/no Rec or M	(9)
				19 yr	M	L	Anterosuperior	5.0×4.0×3.0	S; R+C	1 yr/Rec
10	Kashyap et al, 2004	India	3	8 yr	F	L	Superomedial	NM	B+E+R+C	2 yr/no Rec or M	(10)
				12 yr	F	L	Inferolateral	NM	S	2 yr/no Rec or M
11	Khan and Burke, 2004	USA	1	10 yr	F	L	Contiguous with and indistinguishable from medial rectus muscle	2.0×2.7	S Rec or M	5 yr/no	(11)
12	Chan et al, 2004	China	1	4 yr	M	R	Inferotemporal	3.0	B+S	2 yr/no Rec or M	(12)
13	Lasudry and Heimann, 2000	Belgium	1	2 yr	M	L	Displace or involve the superior rectus/levator muscle complex	NM	B+C+E	1 yr/no Rec or M	(13)
14	Coupland et al, 1991	Germany	1	32 yr	M	L	Among optic nerve, medial and superior rectus muscle	1.6×1.5×1.5	S	4 yr/no Rec or M	(14)
15	Chodankar et al, 1986	India	1	15 yr	M	L	Inferior	2.0×1.0×1.0	S	9 mh/no Rec or M	(15)
16	Font et al, 1982	USA	17	11 mh-69 yr (18 yr)	13 F; 4 M	8 R, 8 L; 1 NM	Not mentioned, 1 case with a figure revealed overlying lateral rectus muscle	NM	B1, B+S+EN1, S5, S+R5, E2, E+R2	3.5–20.6 yr (median 11.4 yr) 10 alive (2 Rec), 2 succumbed to M, 2 lost, 3 succumbed for other reasons	(16)
17	Ishikura et al, 1979	Japan	1	15 mh	F	R	NM	NM	B+E+R	4 yr/no Rec or M	(17)
18	Mukherjee and Agrawal, 1979	India	1	30 yr	M	R	Extending from superior temporal to apex, orbicularis infiltrated	NM	E	Lost	(18)
19	Varghese et al, 1968	India	1	13 yr	F	L	Lateral side, infiltrating lateral rectus muscle	NM	E	A number of mh/Rec	(19)
20	Abrahams et al, 1968	USA	1	55 yr	M	R	Inferior rectus muscle replaced by tumor	2.5×1.8×0.8	E	1 yr/no Rec or M	(20)
21	Altamirano-Dimas and Albores-Saavedra, 1966	Mexico	2	10 mh	M	R	Attached to inferior oblique muscle	3.5×3×2	S	1 yr/Rec succumbed	(21)
				3 yr	F	L	External portion surgery	3.5	S	Succumbed during
22	Nirankari et al, 1963	India	1	38 yr	M	R	NM	3×1.5	S+E+R	1 yr/R, lost	(22)

mh, months; yr, years; B, biopsy; S, surgical excision; E, exenteration; EN, enucleate; R, radiotherapy; C, chemotherapy; Rec, recurrence; M, metastasis; NM, not mentioned.

Table III.

Reported cases in Chinese publications of orbital alveolar soft part sarcoma.

No.	Author, year	Number of cases	Age, years (median)	Sex	Eye affected	Tumour location	Tumour size, cm	Follow-up	Management	(Refs.)
1	Cheng et al, 2013	5	3–19 (8)	4 M, 1 F	3 L, 2 R	Indistinguishable from medial rectus muscle (1); superior rectus muscle (1); lateral rectus muscle (1); inferior rectus muscle (2)	Largest diameter: 2–2.7	9–108 mh (median 52 mh), 4 cases no Rec/M, 1 case Rec	S+EN	(23)
2	Du and Wu, 2012	1	10	F	L	Lateral, indistinguishable from lacrimal gland	1.5	NM	S	(24)
3	Feng et al, 2010	1	2	F	R	Adhering to inferior oblique muscle	2×2	NM	S	(25)
4	Hu et al, 2009	1	8	M	L	Retrobulbar, lateral	NM	NM	NM	(26)
5	He et al, 2004	2	9	F	L	Superotemporal, lateral rectus muscle thickened	2.5×2.3×2	7 yr R; S 0.5 yr no Rec	S+R	(27)
			13	F	L	Retrobulbar, intraconal	2.4×2×1.5	2 mh R; S 0.5 yr no Rec	S+R
6	Dong et al, 2004	1	18	M	R	Retrobulbar, inferomedial, intraconal	2.5×2.8	NM	S	(28)
7	Wang et al, 2003	1	53	M	L	Medially, indistinguishable from medial rectus muscle	4×3	NM	S	(29)
8	Dong et al, 1996	1	25	M	R	Retrobulbar, medially, nodules in lungs and liver	3xx3×1.2	1.3 yr Rec; S+C alive	S	(30)
9	Xu, 1995	1	14	M	L	Apex	NM	NM	B+E	(31)
10	Li et al, 1993	1	20	F	L	Indistinguishable from lateral rectus muscle	2×0.5×0.8	3 yr/no Rec or M	S	(32)
11	Liu, 1989	1	8	F	R	Full of orbit	NM	6.8 yr no Rec/M	S	(33)
12	Wei, 1985	1	23	M	R	NM	NM	4 yr Rec; S 3 yr no R/M	S	(34)
13	Huo et al, 1982	1	10	F	L	Supraorbital	NM	2 mh Rec; S 6 mh no Rec/M	S+E	(35)
14	Ni, 1981	1	20	F	L	NM	NM	6 yr/no Rec/M	E	(36)

mh, months; yr, years; B, biopsy; S, surgical excision; E, exenteration; EN, enucleate; R, radiotherapy; C, chemotherapy; Rec, recurrence; M, metastasis; NM, not mentioned.

Imaging features

Ultrasonography was performed in 4 of the selected cases, which demonstrated hypoechoic inhomogeneous soft tissue masses with increased flow (Fig. 2). A computed tomography (CT) examination revealed well-circumscribed ovoid and enhanced masses in all cases (Fig. 3A). MRI demonstrated that all the tumours exhibited intermediate signal intensity in T1- and T2-weighted images (Fig. 3B and C), in addition to marked enhancement in contrast-enhanced images (Fig. 3D). Imaging features demonstrated that the lesions were located in the medial part of the orbit in 3 cases, in the supraorbital foramen in 2 cases and in the infraorbital foramen in 2 cases, and, in 1 case, the lesion filled the orbital cavity. The tumours were associated with the extraocular muscles (Figs. 2D and 3E-H). Tumours were located intramuscularly in 3 cases, indistinguishable from the muscles in 3 cases and abutting the muscles in 2 cases. The average largest diameter of the masses was 3.6 cm (range, 2.0–5.0 cm).

Figure 2.

Ultrasonography imaging of alveolar soft part sarcoma. (A) A-scan ultrasonography of case 2 demonstrated low to moderate internal reflectivity with a high velocity peak. (B) B-scan ultrasonography of case 2 revealed a hypoechoic, homogeneous soft tissue mass indenting the globe. (C) Colour Doppler flow imaging of case 2 revealed marked increased blood flow within the mass. (D) B-scan ultrasonography of case 1 revealed a hypoechoic, homogeneous soft tissue mass. The arrow indicates the attachment point of the medial rectus muscle. The mass had an association with the medial rectus muscle.

Figure 3.

CT and MRIs of alveolar soft part sarcoma. (A) Coronal section of CT imaging of case 5 showing a well-defined homogeneous mass with equal density to muscle in the left orbit. It was indistinguishable from the superior rectus/levator muscle complex with marked downward displacement of the globe. (B) Coronal T1-weighted MRI of case 5 revealed an ovoid isointense mass in the left medial superior orbit that was indistinguishable from the superior rectus/levator muscle complex with marked downward displacement of the globe. (C) Coronal T2-weighted MRI of case 5 revealed an ovoid isointense mass in the left medial superior orbit. (D) Coronal contrast-enhanced and fat-suppressed T1-weighted MRI of case 5 revealed an ovoid mass with marked enhancement in the left medial superior orbit. (E) Axial T1-weighted MRI of case 3 revealed an ovoid isointense mass in the inferior part of the right orbit indistinguishable from the inferior rectus muscle throughout its length to the apex with marked upward displacement of the globe. (F) Coronal T2-weighted MRI of case 3 revealed an ovoid isointense mass in the inter-inferior part of the right orbit indistinguishable from the inferior rectus muscle with marked out-upward displacement of the globe. (G) Coronal T1-weighted MRI of case 4 revealed an ovoid isointense mass in the left superior orbit indistinguishable from the superior rectus muscle with marked downward displacement of the globe. (H) Coronal T1-weighted MRI of case 1 revealed an ovoid isointense mass in the medial part of the right orbit indistinguishable from the medial rectus muscle with marked outward displacement of the globe. CT, Computed tomography; MRI, magnetic resonance imaging.

Histopathological features

As presented in Fig. 4, overall, these poorly circumscribed pale grey or grey-yellow masses were soft and friable, tending to haemorrhage (Fig. 4A). Microscopic examination identified that the characteristic arrangement of the tumour cells was organoid, in a nesting or alveolar pattern, which was more obvious at low magnification. The size and appearance of the nests tended to be uniform. The tumour cell nests were separated by delicate septa of connective tissue containing sinusoidal vascular channels lined by flattened endotheliocytes. The large oval or polygonal tumour cells had a distinctly epithelioid appearance with somewhat similar size and shape. The cell borders were sharply defined. There were 1 or 2 large vesicular nuclei with prominent nucleoli per cell. Nuclear atypia was not common. Eosinophilic cytoplasm was abundant, with a finely granular, transparent or vacuolar pattern (Fig. 4C). Mitotic figures were uncommon. All cases were positive for diastase following PAS staining (Fig. 4D), although this may not have been apparent from H&E staining. Tumour emboli could be observed in the small vessels in the tumour tissue of cases 4 and 5. Cases 2, 3 and 4 were positive for vimentin by immunohistochemistry. Cases 1, 6 and 7 had desmin-positive foci (Fig. 4F). Smooth muscle actin was positive in a number of tumour cells in case 6. Transcription factor binding to immunoglobulin heavy-chain enhancer 3 (TFE3) was positive in all cases with the exception of case 3 (Fig. 4G). Cluster of differentiation (CD) 147 was positive in all cases. Other markers, including cytokeratin, epithelial membrane antigen (EMA), carcinoembryonic antigen, actin, neuron-specific enolase (NSE), synaptophysin, chromogranin A, S-100 protein, melanoma, melan A, CD99, CD34 and α-fetoprotein, were negative in all cases. The antigen Ki-67 proliferation index was <10% in the majority of cases, but was 15% in cases 2 and 3 (Fig. 4H; Table IV).

Figure 4.

Histopathological examination of alveolar soft part sarcoma. (A) Gross examination of the histopathological specimen revealed an encapsulated mass measuring 2.5×1.5×1.5 cm. It had adhered to the medial rectus muscle of the right eye and extended to the apex. (B) Image of tissue from case 7 showing the association between the tumour and the extraocular muscle. The left top of the fig. is the tumour and the remaining muscle is located at the low right (H&E; magnification, ×50). (C) Image of tissue from case 5 demonstrating nesting or organoid arrangement separated by delicate partitions of fibrous connective tissue, which formed a characteristic pseudoalveolar pattern. Blood sinusoid was easily observed between the nests. The individual tumour cells were round or polygonal with abundant eosinophilic and finely granular cytoplasm and those at the nest centre were sparse. Nuclear atypia was not obvious (H&E; magnification, ×200). (D) PAS stain with diastase digestion of tissue from case 7 exhibited the characteristic PAS-positive pruinose crystalline inclusions in the cytoplasm of certain tumour cells (indicated by arrow). (PAS; magnification, ×400). (E) Image of tissue from case 6 showing strong membrane immunoreactivity of CD147 in certain tumour cells (DAB; magnification, ×400). (F) Desmin immunostaining identified focal cytoplasmic immunoreactivity in tissue from case 7 (DAB; magnification, ×400). (G) The transcription factor for immunoglobulin heavy-chain enhancer 3 immunostaining of tissue from case 6 demonstrated specific marked nuclear immunoreactivity in certain tumour cells (DAB; magnification, ×200). (H) Immunostaining of tissue from case 3 revealed nuclear immunoreactivity for Ki-67 in certain tumour cells (DAB; magnification, ×400). PAS, periodic acid-Schiff; CD, cluster of differentiation; DAB, 3,3′-diaminobenzidine; H&E, haematoxylin and eosin.

Table IV.

Immunohistochemical results of the patients with orbital alveolar soft part sarcoma.

Case	Immunohistochemical result
1	Vimentin− desmin focus+ actin− CK− NSE− Syn− CgA− S-100− TFE3++ CD147+ Ki-67+5%
2	Vimentin focus+ desmin− CK− NSE− Syn− CgA− S-100− CEA− TFE3++ CD147+ Ki-67+15%
3	Vimentin+ desmin− SMA− actin− CK− EMA− NSE− Syn− CgA− S-100− HMB45− CEA− AFP− CD34− CD31− TFE3− CD147+ Ki-67+15%
4	Vimentin+ desmin− actin− CK− NSE− Syn− CgA− S-100− HMB45− AFP− CD34− CD99− TFE3++ CD147+ Ki-67+5%
5	Vimentin− desmin− CK− Syn− CgA− S-100− Mela A− SMA− CD34− CD99− TFE3++ CD147+ Ki-67+5%
6	Vimentin− desmin partly+ CK− NSE− Syn− CgA− S-100− AFP− SMA partly+ CD34++ TFE3++ CD147+ Ki-67+10%
7	Vimentin− desmin partly+ CK− NSE− Syn− CgA− S-100− AFP− SMA− CD34++ TFE3+++ CD147+ Ki-67+8%
8	Vimentin− desmin− Myogenin− CK− NSE− Syn− CgA− S-100− CD56− CD34− TFE3++ CD147+ Ki-67+5%

CK, cytokeratin; NSE, neuron-specific enolase; Syn, synaptophysin; CgA, chromogranin A; TFE3, transcription factor for immunoglobulin heavy-chain enhancer 3; CD147, cluster of differentiation 147.

Treatment and follow-up

Cases 1, 3, 4, 5 and 8 underwent surgical excision of the tumour, cases 2 and 6 underwent orbital exenteration, and case 7 underwent partial orbital exenteration. Cases 1, 2, 4, 5, 6 and 8 received postoperative local radiotherapy on the orbital region. Cases 6 and 8 received chemotherapy. Case 1 was doing well at 6 months and was then lost to follow-up. Cases 4, 5, 6, 7 and 8 were doing well with no evidence of local recurrence or metastasis during the follow-up period (between 3 and 61 months). Local recurrence of the tumour developed at 3 months post-tumorectomy in case 3, with the patient succumbing 1 year after being withdrawn from treatment by the patient's parents. Case 2 visited the hospital presenting with recurrence of the tumour 3 months after undergoing tumorectomy at another hospital. A doctor advised orbital exenteration, which the patient declined, instead opting to undergo excision of the tumour only. Local recurrence developed again after 3 months. CT and MRI demonstrated that the orbital cavity was occupied by the tumour. The patient underwent orbital exenteration. The tumour was recurrent 3 months after surgery and the patient received radiotherapy. The patient complained of gradually aggravated headaches after 1 month. MRI demonstrated invasion to the sphenoid bone. The patient eventually succumbed.

The median period of follow-up following surgical treatment was 12 months (range, 3–61 months) in the series of the present study, whereas the period was 12 months (range, 2–247 months) in the PubMed literature (Table II) and 48 months (range, 2–108 months) in the Chinese literature (Table III). In the 65 patients with follow-up data, 43 (66.2%) were alive with no evidence of disease during the follow-up period, 12 patients (18.5%) were alive with local recurrence, and 2 (3.1%) exhibited metastases to the lungs and liver. Certain patients (n=4; 6.2%) succumbed to metastatic disease and 4 (6.2%) succumbed to non-related causes.

Discussion

Alveolar soft part sarcoma (ASPS) is a rare tumour primarily affecting children and adolescents. There is a slight female preponderance in adults (60% of patients are female) (37), which is not observed in children (38). ASPS predominantly affects the deep soft tissues of the extremities in adults, particularly the thighs and buttocks; the arms, thorax and retroperitoneum are seldom involved (39). The most common location in children is the head and neck region, particularly the orbit and tongue (16,40). Following the review of hundreds of reports, it was identified that, in 172 cases, orbital involvement had the second-highest incidence (15.1%), following the buttock and thigh, and that orbital involvement had the highest incidence in ASPS arising in the head and neck region (55%) (41).

Characteristics of orbital ASPS

From these data, it was concluded that orbital ASPS has characteristics distinct from those of ASPS arising in other locations: i) Orbital ASPS involves a younger population; the median age of the patients when ASPS is diagnosed in locations other than the orbit was >30 years (42,43), whereas that of patients with orbital ASPS is <15 years; ii) the course of disease is usually shorter in orbital ASPS since the symptoms are easily noticed by the patient or parents, therefore: i) Tumour size in orbital ASPS is frequently smaller than ASPS arising in other locations. The median size of orbital ASPS is usually <5 cm, whereas that in other locations is >5 cm (5,42).

Clinical features

Orbital ASPS has no defining clinical features. As with other space-occupying lesions in the orbit, patients with ASPS primarily present with proptosis, abnormal position of the eyes, eyelid swelling, and conjunctival congestion with dilated and tortuous vessels (16). In certain cases, metastasis to the lungs or brain may be the presenting feature of ASPS (44).

Imaging features

Ultrasonography of ASPS is non-specific, but often reveals a slightly hypoechoic or hyperechoic and heterogeneous soft tissue mass with markedly increased blood flow. CT usually demonstrates a soft tissue mass that is homogeneous and isodense to muscle with vigorous enhancement. Reports in the literature on MRI of this tumour have identified intermediate or hyperintense signal intensity in T1-weighted images and hyperintense signal intensity in T2-weighted images. The majority of lesions exhibit marked intense enhancement in contrast-enhanced MRI (45,46). A number of studies have focused on the characteristic imaging features of orbital ASPS. In the present series of cases analysed, all the lesions demonstrated intermediate signal intensity in T1- and T2-weighted images, the majority with marked enhancement in contrast-enhanced images.

Diagnosis and differential diagnosis

There are no distinct characteristics in the clinical and imaging features of this kind of tumour. Owing to the high vascularization, the tumour may be misinterpreted as a type of vasogenic tumour, including hemangioma, lymphangioma or hemangiopericytoma, by clinicians prior to surgery (47). The final diagnosis should be dependent on the pathological examination following surgery. The pathomorphological features of ASPS should allow for differential diagnosis from other tumours, including paraganglioncytoma, granular cell tumour, amelanotic melanoma, alveolar rhabdomyosarcoma and metastatic renal cell carcinoma (48). PAS is an important stain for the diagnosis of ASPS, as ASPS possesses PAS-positive diastase-resistant granules in >80% of cases (49). All the present cases were PAS-positive. Immunohistochemical examination is also important for differential diagnosis. The majority of ASPS tumour cells exhibit moderate to strong nuclear staining of TFE3, which is a sensitive and specific marker for ASPS. Monocarboxylate transporter protein 1 and its cellular chaperone protein CD147 also demonstrate positive reactions in PAS-positive diastase-resistant cells. There are no other specific markers for ASPS, which does not express the common antigens of the epithelium (e.g. cytokeratin and EMA), neuroendocrine cells (e.g. NSE, synaptophysin, chromogranin and S-100 protein) or melanocytes (e.g. human melanoma black-45 and melan A). However, certain markers are positive in the aforementioned tumours, allowing for differential diagnosis. The representative pathological features combined with supplementary examinations, including immunohistochemical staining, PAS staining and molecular biology technologies, are useful for the pathological and differential diagnosis of ASPS.

Histogenesis of the tumour

The histogenesis of ASPS has been controversial for a number of years. Genetic studies on ASPS have confirmed a specific fusion gene involving the ASPS critical region-1 gene and TFE3 and the resultant fusion protein generated by the unbalanced chromosomal translocation [der(17)t(X:17)(p11;25)] (50). Therefore, it is generally accepted that ASPS is a sarcoma associated with chromosomal translocation, therefore it is sorted into a class containing uncertain differentiated tumours.

It was hypothesized for a number of years that ASPS represented an unusual form of myogenic tumour (51–53). Subsequently, conflicting results on the expression of muscle-associated markers have disproved this hypothesis (54,55). Previously, genetic expression profiles of ASPS identified that certain muscle-specific transcripts were increased, which suggests an association with muscle cell progenitors (56). ASPS has a marked predilection to arise on the thighs, buttocks and abdominal or chest walls, which suggests that ASPS is associated with skeletal muscles or musculofascial planes (37). The present series and the cases reviewed revealed that orbital ASPS is generally associated with the extraocular muscles. There were 19 and 9 patients in Tables II and III respectively, whose tumours had been mentioned definitely to be abutting, adhering to or indistinguishable from the extraocular muscles. In the present series, the tumours were clearly observed during the surgical procedures. The tumours were revealed following longitudinally splitting the thickened extraocular muscles in 3 cases, whereas the tumours grew along with and were indistinguishable from the extraocular muscles in 3 cases. There were 6 cases expressing vimentin or desmin in the present series, which were identified using immunohistochemistry. Although immunohistochemical examination of muscle-associated markers in previous years did not demonstrate myogenic histogenesis, the growth pattern of this tumour suggests that orbital ASPS is associated with the extraocular muscles.

Treatment

Generally, complete surgical excision of the localized tumour with a microscopically negative margin is the established treatment for ASPS. The possibility of recurrence is rare if the lesion has been completely resected (57). The pathological status of surgical margin, which indicates whether active tumour tissue remains, is important for prognosis. Surgery is also the primary treatment in orbital ASPS; however, due to the narrow space and complex organization of the orbit, it is occasionally impossible to perform a complete resection if the patient declines to undergo an exenteration. Previous studies have demonstrated that chemotherapy and radiotherapy do not improve the survival rate; however, radiotherapy as an adjuvant therapy has been demonstrated to decrease the risk of local recurrence (50,58). Metastasectomy may markedly prolong the survival rate of patients with pulmonary metastases of ASPS (16,37).

Prognosis

It has been reported that the biological behaviour of ASPS is relatively indolent, with the 2-, 5-, 10- and 20-year overall survival rates being 77, 60, 38 and 15%, respectively (37). Metastases occur most commonly in the lungs, brain and bones (37). Since ~1/3 patients develop metastases to the lungs or brain decades after initial diagnosis, long-term follow-up is strongly advised for all cases of ASPS.

According to previous studies, the patient's age, tumour size and presence of metastases at diagnosis are significant prognostic factors in ASPS. It is hypothesized that younger age with a tumour size of <5 cm and absence of metastases is associated with a more favourable outcome (48,59). If the tumour is resected completely, younger patients may achieve a good prognosis with prolonged survival rates (40,60). Certain studies have reported 100% survival rates beyond 5 years in paediatric patients (38). However, there was an exception in the present series: A 2-year-old patient succumbed 1 year after diagnosis, possibly due to the large tumour and withdrawal from therapy.

The prognosis is improved in patients with ASPS located in the orbit and tongue, which is possibly associated with smaller lesions, younger age at diagnosis and shorter course of disease (16,40), which was also demonstrated in the present review.

It is known that there are no histopathological features predictive of prognosis in ASPS (48). However, in the present series, 2 cases (cases 2 and 3) recurred shortly following surgery (<3 months). Of these, 1 patient succumbed 1 year later and the other had an invasion to the brain that was possibly fatal. It is notable that the Ki-67 proliferation index was 15% in these 2 cases, whereas it was ≤10% in 5 cases, suggesting that the Ki-67 proliferation index may be associated with ASPS prognosis. Further study is required in order to investigate this association.

In conclusion, orbital ASPS exhibits characteristics that are distinct from those of ASPS arising in other locations. Orbital ASPS usually affects a younger population, the course of disease is shorter and the tumour size is smaller. Therefore, the prognosis is improved in orbital ASPS. Orbital ASPS may have an association with the extraocular muscles and the Ki-67 proliferation index may be associated with prognosis of ASPS.

Glossary

Abbreviations

ASPS

alveolar soft part sarcoma

CT

computed tomography

MRI

magnetic resonance imaging

PAS

periodic acid-Schiff

SMA

smooth muscle actin

TFE3

transcription factor for immunoglobulin heavy-chain enhancer 3

EMA

epithelial membrane antigen

CEA

carcinoembryonic antigen

NSE

neuron-specific enolase

AFP

α-fetoprotein