True Hemangiopericytoma of the Nasal Cavity.
Since first reported by Stout and Murray, hemangiopericytomas have been accepted as soft tissue tumors with distinct clinicopathologic features. They are characterized as benign or malignant, round to spindle cell tumors with numerous "staghorn" branching vascular channels. Another characteristic is the difficulty encountered in predicting their clinical behavior.[1-4] The cellular differentiation of hemangiopericytomas has been questioned recently, because they commonly lack the immunohisto-chemical and electron microscopic differentiation properties of pericytes.[5-8] Indeed, the hemangiopericytoma-like pattern is a nonspecific feature observed in various soft tissue tumors. Thus, hemangiopericytoma has become a nonspecific diagnosis rather than a specific concept indicating cellular differentiation.
Sinonasal hemangiopericytomas, which were also described by Stout, are thought to be distinct from hemangiopericytomas of the soft tissues because of their excellent prognosis and uniform cellular features. Compagno et al described this entity as "hemangiopericytoma-like tumor" as early as 1976, and Fletcher recently pointed out that sinonasal hemangiopericytomas are tumors with true pericytic myoid differentiation distinct from soft tissue hemangiopericytomas.
In this article, we present 2 cases of nasal hemangiopericytoma with conspicuous pericytic myoid differentiation, which seem to be intimately related to perivascular myoma. We also review cases reported previously as sinonasal hemangiopericytoma, hemangiopericytoma-like tumor, and glomus tumor and attempt to classify these cases into distinct clinicopathologic entities.
MATERIALS AND METHODS
Tissue specimens from 2 patients were fixed in formalin, embedded in paraffin, and stained with hematoxylin-eosin and silver impregnation stain. The streptavidin-biotin-peroxidase complex method (SABC kit, Dako, Kyoto, Japan) was used for immunohistochemistry. The primary antibodies and their final dilutions were anti-desmin (D33, Dako, 1:50), anti-[Alpha]-smooth muscle actin (Dako, 1:200), anti-muscle actin (HHF-35, Enzo Diagnostics, New York, NY, 1:8000), CD34 (NU-4A1, Nichirei, Tokyo, Japan, 1:100), and anti-high-molecular-weight caldesmon (Dako, 1:50). Microwave pretreatment was performed for desmin and high-molecular-weight caldesmon analyses. The nuclei were counterstained with hematoxylin. Fresh tissue from case 1 was fixed in 2% glutaraldehyde and then embedded in epoxy resin. Ultrathin sections were stained with uranyl acetate and lead citrate and were observed using a JEM 1200EX transmission electron microscope (JEOL Ltd, Tokyo, Japan).
REPORT OF CASES
A 78-year-old woman was admitted to the hospital complaining of right nasal obstruction and hemorrhage. Rhinoscopic examination disclosed a slightly red polypoid tumor covered by mucosa. The tumor grew slowly, and 3 months after her first admission a polypectomy was performed. The tumor arose from the right nasal septum and was extirpated together with neighboring normal mucosa. The tumor was approximately 25 mm in its maximum length. This was a recent case, and as of 4 months' follow-up there had been no recurrence.
A 60-year-old man was admitted to the hospital with a complaint of nasal hemorrhage. A right nasal polyp arising from the septum was observed under the rhinoscope. The polyp was extirpated piece by piece. The tumor recurred 1 year later and was re-extirpated with neighboring normal mucosa. The histology of the recurrent tumor was unchanged from that of the primary tumor. The patient's postoperative course has been uneventful for 8 years.
Both tumors exhibited polypoid growth covered by normal, respiratory epithelium (Figure 1). The tumors were composed of uniform, rather eosinophilic short spindle or small stellate cells with indistinct cytoplasmic borders (Figures 2 and 3). The round to oval, uniform nuclei did not show atypia. The spindle cells tended to be arranged in short narrow fascicles. In case 1, concentric cellular configurations were occasionally seen (Figure 1). The tumors were rich in thin or dilated venule-like vessels, but staghorn-like vessels were rarely seen. There was sparse infiltration of a few lymphocytes and mast cells. Mitoses were rare and were seen only in case 1. Although silver impregnation stain disclosed numerous reticulum fibers between the tumor cells, they were thin and delicate and did not surround the individual cells clearly.
Both tumors were diffusely positive for vimentin. [Alpha]-Smooth muscle actin and muscle actin (HHF-35) were also diffusely immunolabeled in both tumors, except for the concentric cellular area seen in case 1 (Figure 4). Neither tumor was positive for desmin, CD34, or high-molecular-weight caldesmon.
Ultrastructurally, there were 2 cell types: spindle-shaped cells and stellate cells. Cells surrounding the blood vessels were clearly separated by basement membrane from nonneoplastic endothelial cells. Occasionally, stellate cells formed a concentric configuration, as seen by light microscopy. The spindle tumor cells had many mitochondria, free ribosomes, and rough endoplasmic reticulum and were surrounded by discontinuous, irregularly thickened basement membrane. Characteristically, they contained a bundle of microfilaments with fusiform dense bodies and subplasmalemmal plaques (Figure 5). In contrast, the stellate tumor cells in the circular concentric structure had numerous cytoplasmic processes and mitochondria, and scattered Golgi apparatus. Although microfilaments were inconspicuous in these cells, perinuclear bundles of intermediate filaments were evident. Well-developed intercellular junctions were observed in both cell types. Pinocytotic vesicles were not observed.
Recently, Granter et al described distinctive tumors showing perivascular proliferations of small spindle and round cells with myoid differentiation as "perivascular myomas." They subdivided the tumors into myofibromatosis, glomangiopericytoma, and myopericytoma types, but these forms are interrelated and frequently indistinguishable. Perivascular myomas exhibit a broad histologic spectrum, from hemangiopericytoma-like or glomus tumor-like to angioleiomyoma-like, and it is speculated that they differentiate along the lines of smooth muscle, pericytic, and glomus cells. Immunohistochemically, perivascular myomas are stained frequently with anti-actin antibodies and rarely with anti-desmin antibodies, according to their degree of cellular differentiation.
The tumors presented here, one of which was examined by electron microscopy, are thought to belong to a lineage above perivascular myoid cells, based on their features such as small spindle or stellate cells, abundance of various-sized blood vessels, intense immunoreactivity for [Alpha]-smooth muscle actin, and well-developed bundles of microfilaments with dense bodies. Furthermore, these tumors are distinctive in the sense that under light microscopy they are composed of more uniform tumor cells, lacking glomus tumor or myofibroblastic-like differentiation. These characteristics suggest that such tumors may be a pure form of hemangiopericytoma, which is thought to be situated at one end of the broad spectrum of perivascular myomas.
Stout, together with Murray,[1,3] first reported hemangiopericytomas and noticed their great variety of cellular and structural features. This variety was explained by the hypothesis that pericytes are related to smooth muscle cells, and therefore hemangiopericytomas can consist of cells that are incomplete smooth muscle-like to epithelioid glomus tumor-like. However, it has become clear that hemangiopericytoma-like features are encountered in various soft tissue tumors and that soft tissue hemangiopericytomas generally lack pericytic differentiation, both ultrastructurally and immunohistochemically.[5-7] Thus, hemangiopericytomas now tend to be recognized as heterogeneous tumors with various cellular differentiation.
Although hemangiopericytomas arising from sites other than soft tissues are rare,[1,3,4] more than 60 cases of sinonasal hemangiopericytoma have been described in the literature since the first report by Stout.[3,9,10,12-26] Because sinonasal hemangiopericytomas are frequently composed of more uniform, smaller cells and show excellent prognosis compared with the soft tissue types, it has been suggested that they may be distinct from soft tissue hemangiopericytoma. Compagno et al used the designation hemangiopericytoma-like tumor as early as 1976. In contrast, based on ultrastructural and immunohistochemical findings, Eichhorn et al suggested that nasal hemangiopericytoma does not differ from similar tumors in other locations. However, they observed focal smooth muscle actin immunoreactivity in nasal tumors, suggesting myoid differentiation, which is exceptional in soft tissue hemangiopericytomas. Recently, Fletcher concluded that sinonasal hemangiopericytoma is the only tumor showing convincing pericytic differentiation among the hemangiopericytomas that arise in adulthood.
We reviewed the cases of sinonasal hemangiopericytomas reported previously in the literature[3,9,10,12-26] and found at least 3 histologic subtypes. The first subtype consists of tumors that are identical to soft tissue hemangiopericytomas composed of rather plump spindle cells with various degrees of nuclear atypia. At least 6 cases reported by Stout, Murashima, Lenczyk et al, Benveniste et al, Gudrun, and Tsuneyoshi et al, and some of the 11 cases reported by Eichhorn et al, appear to be of this type (Table). Myoid differentiation was not confirmed in this type as well as in the soft tissue-type hemangiopericytomas. As expected, the tumors in these cases were frequently aggressive, and fatal cases were not uncommon.[3,9,12,15,19,22] Very recently, intimate relationships between hemangiopericytoma and solitary fibrous tumor have been reported. It is important to differentiate these tumors, because most solitary fibrous tumors of the soft tissue are benign. CD34 is an extremely useful marker for this purpose.[27,28]
Review and Subclassification of Sinonasal Hemangiopericytoma and Hemangiopericytoma-like Tumor(*) Year Age, y/ Size, Source Published Sex Site mm Soft tissue--type hemangiopericytoma Stout 1949 66/F Ethmoid sinus ... Murashima 1961 4/F Nasal cavity ... Lnczyk 1968 35/M Nasal cavity ... Benveniste 1973 24/M Ethmoid sinus ... and Harris Gudrun 1979 61/M Ethmoid sinus ... Tsuneyoshi 1984 31/F Nasal cavity ... et al Eichhorn et 1990 42/F Maxillary sinus ... al (case 6) True hemangiopericytoma Compagno and 1976 42-79/ Nasal cavity, 20-70 Hyams 9M, 14F n = 13 (23 cases) Ethmoid, n = 7 Sphenoethmoid, n = 3 Batsakis et 1983 79/F Nasal cavity 30 al Eichhorn et 1990 50/F Middle 21 al (case 8) turbinate Present case 1 2001 78/F Nasal cavity 25 Present case 2 2001 60/M Nasal cavity Source Spread Treatment Soft tissue--type hemangiopericytoma Stout Orbit Excision Murashima Nasal septum, Incomplete nasopharynx excision Lnczyk Cribriform palate Local excision Craniotomy Benveniste None Partial and Harris ethmoidectomy Cryosurgery Gudrun Nasopharynx, Lateral rhinotomy frontal sinus, Radiation nasal cavity, anterior cranial fossa Tsuneyoshi ... ... et al Eichhorn et Nasal cavity, Radiation al (case 6) retrobulbar area, sphenoid sinus True hemangiopericytoma Compagno and ... Excision, n = 8 Hyams Ethmoidectomy, (23 cases) n = 7 Sphenoidectomy, n = 3 Polypectomy, n = 1 Radiation, n = 3 Batsakis et Ethmoid Excision by al forceps Eichhorn et None Polypectomy al (case 8) Present case 1 None Excision Present case 2 None Polypectomy Recurrence No. Source (Interval) Follow-up Soft tissue--type hemangiopericytoma Stout 4 DOD Murashima DOD, 3 wk Lnczyk 3 (2, 4, 6 y) AWOD, 2 y Benveniste 1 (1 y) AWOD, 2.5 y and Harris Gudrun None AWOD, 18 mo Tsuneyoshi 1 DOD, 1.5 y et al Eichhorn et 1 (6 y) AWD, 3 y al (case 6) True hemangiopericytoma Compagno and 2 cases, (6 AWOD, 22 Hyams and 11 y) cases, 6 mo (23 cases) to 19 y; recurrence in 2 cases; 1 case lost to follow-up Batsakis et 1 (2 y) AWOD, 2 y al Eichhorn et 1 (17.5 y) AWOD, 2.5 y al (case 8) Present case 1 Recent case Present case 2 1 (1 y) AWOD, 8 y (*) Ellipses indicate unknown; DOD, died of disease; AWOD, alive without disease; and AWD, and alive with disease.
The second subtype includes true hemangiopericytoma tumors, similar or almost identical to the present cases, which are composed of uniform spindle or stellate cells and which exhibit various degrees of myoid differentiation mimicking normal pericytes.[7,29] Previously reported cases that seem to be of the true hemangiopericytoma type, based on the histologic descriptions and microphotographs, are summarized in the Table.[10,24,26] Compagno et al analyzed the largest series, which included 23 cases. Although immunohistochemical and electron microscopic examinations were not included in their study, we believe most of these cases are of the true hemangiopericytoma type, based on their distinctive uniform histologic features. We think that at least 1 (case 8) of the 11 cases described by Eichhorn et al also is of true hemangiopericytoma type, because of its histologic features and actin immunopositivity. Although some of 10 cases reported by Gorenstein et al also seem to be perivascular myomas, unfortunately the clinical details are unclear. One case reported by Batsakis et al is a convincing case of true hemangiopericytoma from the clearly depicted light and electron microscopic features showing well-developed myofilaments with dense bodies, as pointed out by Fletcher. These tumors occasionally recur locally, but no case with an adverse outcome has been reported.
The third subtype consists of tumors intimately related to glomus tumors. Sinonasal glomus tumors are extremely rare, and only 6 cases have been reported in the English literature to date, excluding the paragangliomas reported as glomus tumors in an old series.[18,30-34] The histology ranges from a typical glomus tumor composed of compact epithelioid cells to tumors indistinguishable from perivascular myoma.[31,32,34] In contrast, some tumors reported as sinonasal hemangiopericytoma seem to closely resemble glomus tumor. Glomus and glomuslike tumors and true hemangiopericytomas, if not identical with respect to degree of myoid differentiation as judged by electron microscopy, are likely to belong to one cellular spectrum. In their biological behavior, these tumors seem to be almost benign, like true hemangiopericytoma. Recently, glomus tumors of the soft tissue were demonstrated to constantly express high-molecular-weight caldesmon, which does not exist in normal pericytes.[35,36] It may be useful to analyze the differences between glomus tumors and pericytic tumors in the future.
In summary, the immunohistochemical and ultrastructural features of 2 cases of nasal hemangiopericytoma are described. They are identical to tumors formerly reported as hemangiopericytoma-like tumors and are thought to be true hemangiopericytomas. So-called sinonasal hemangiopericytomas reported in the past include different histologic types, and sinonasal true hemangiopericytoma should be differentiated from soft tissue-type hemangiopericytoma because of its far better prognosis.
[1.] Stout AP, Murray MR. Hemangiopericytoma: a vascular tumor featuring Zimmermann's pericytes. Ann Surg. 1942;116:26-33.
[2.] Enzinger FM, Weiss SW. Soft Tissue Tumors. 3rd ed. St Louis, Mo: CV Mosby Co; 1995:713-733.
[3.] Stout AP. Hemangiopericytoma: a study of twenty-five new cases. Cancer. 1949;2:1027-1054.
[4.] O'Brien P, Brasfield RD. Hemangiopericytoma. Cancer. 1965;18:249-252.
[5.] Nunnery EW, Kahn LB, Reddick RL, Lipper S. Hemangiopericytoma: a light and ultrastructural study. Cancer. 1981;47:906-914.
[6.] Dardick I, Hammar SP, Schneithauer BW. Ultrastructural spectrum of hemangiopericytoma: a comparative study of fetal, adult, and neoplastic pericytes. Ultrastruct Pathol. 1989;13:111-154.
[7.] Schurch W, Skalli O, Lagace R, Seemayer TA, Gabbiani G. Intermediate filament protein and actin isoform as markers for soft-tissue tumor differentiation and origin, III: hemangiopedcytomas and glomus tumors. Am J Pathol. 1990;136: 771-786.
[8.] Fletcher CDM. Hemangiopericytoma: a dying breed? Reappraisal of an `entity' and its variants: a hypothesis. Curr Diagn Pathol. 1994;1:19-23.
[9.] Tsuneyoshi M, Dimaru Y, Enjoji M. Malignant hemangiopericytoma and other sarcomas with hemangiopericytoma-like pattern. Pathol Res Pract. 1984; 178:446-453.
[10.] Compagno J, Hyams VJ. Hemangiopericytoma-like intranasal tumors: a clinicopathologic study of 23 cases. Am J Clin Pathol. 1976;66:672-683.
[11.] Granter SR, Badizadegan K, Fletcher CDM. Myofibromatosis in adults, glomangiopericytoma, and myopericytoma: a spectrum of tumors showing perivascular myoid differentiation. Am J Surg Pathol. 1998;22:513-525.
[12.] Murashima J. Case of hemangiopericytoma originating in nasal cavity and nasal sinus of small child. Otolaryngology (Japanese). 1961;33:537-539.
[13.] Rhodes RE, Brown HA, Harrison EG Jr. Hemangiopericytoma of nasal cavity. Arch Otolaryngol. 1964;79:505-511.
[14.] Gill BS, Mehra YN. Haemangiopericytoma in nasal cavity. J Laryngol Otol. 1968;82:839-844.
[15.] Lenczyk IM. Nasal hemangiopericytoma. Arch Otolaryngol. 1968;87:110-113.
[16.] Eneroth CM, Fluur E, Soderberg G, Anggard A. Nasal hemangiopericytoma. Laryngoscope. 1970;80:17-24.
[17.] Alli AF, Singh SP. Haemangiopericytoma of the nasal cavity in Ibadan, Nigeria. J Laryngol Otol. 1972;86:405-410.
[18.] DeBord BA. Unusual presentations in otolaryngology. Surg Clin North Am. 1972;52:473-483.
[19.] Benveniste RJ, Harris HE. Nasal hemangiopericytoma. Arch Otolaryngol. 1973;98:358-359.
[20.] Hahn MJ, Dawson R, Esterly JA, Joseph D. Hemangiopericytoma: an ultrastructural study. Grocer. 1973;31:255-261.
[21.] Gorenstein A, Facer GW, Weiland LH. Hemangiopericytoma of the nasal cavity. Otolaryngology. 1978;86:405-415.
[22.] Gudrun R. Haemangiopericytoma in otolaryngology. J Laryngol Otol. 1979;93:477-494.
[23.] De Campora E, Calabrese V, Bianchi PM, Camaioni A, Corradini C. Malignant hemangiopericytoma of the nasal cavity: report of a case and review of the literature. J Laryngol Otol. 1983;97:963-968.
[24.] Batsakis JG, Jacob JB, Templeton AC. Hemangiopericytoma of the nasal cavity: electron-optic study and clinical correlations. J Laryngol Otol. 1983;97: 361-368.
[25.] Chawla OP, Oswal VH. Haemangiopericytoma of the nose and paranasal sinuses. J Laryngol Otol. 1987;101:729-737.
[26.] Eichhorn JH, Dickersin GR, Bhan AK, Goodman ML. Sinonasal hemangiopericytoma: a reassessment with electron microscopy, immunohistochemistry, and long-term follow-up. Am J Surg Pathol. 1990;14:856-866.
[27.] Suster S, Nascimento AG, Miettinen M, Sickel JZ, Moran CA. Solitary fibrous tumors of soft tissue: a clinicopathologic and immunohistochemical study of 12 cases. Am J Surg Pathol. 1995;19:1257-1266.
[28.] Hasegawa T, Hirose T, Seki K, et al. Solitary fibrous tumor of the soft tissue: an immunohistochemical and ultrastructural study. Am J Clin Pathol. 1996;106: 325-331.
[29.] Skalli O, Pelte MF, Peclet MC, et al. [Alpha]-Smooth muscle actin, a differentiation marker of smooth muscle cells, is present in microfilamentous bundles of pericytes. J Histochem Cytochem. 1989;37:315-321.
[30.] Pantazopoulos PE. Glomus tumor (glomangioma) of the nasal cavity. Arch Otolaryngol. 1965;81:83-86.
[31.] Fu Y, Perzin KH. Non-epithelial tumors of the nasal cavity, paranasal sinuses, and nasopharynx: a clinicopathologic study, I: general features and vascular tumors. Cancer. 1974;33:1275-1288.
[32.] Potter AJ Jr, Khatib G, Peppard SB. Intranasal glomus tumor. Arch Otolaryngol. 1984;110:755-756.
[33.] Hayes MMM, Van der Westhuizen N, Holden GP. Aggressive glomus tumor of the nasal region: report of a case with multiple local recurrences. Arch Pathol Lab Med. 1993;117:649-652.
[34.] Chu PG, Chang KL, Wu AY, Weiss LM. Nasal glomus tumors: report of two cases with emphasis on immunohistochemical features and differential diagnosis. Hum Pathol. 1999;30:1259-1261.
[35.] Watanabe K, Kusakabe T, Hoshi N, Saito A, Suzuki T. h-Caldesmon in leiomyosarcoma and tumors with smooth muscle cell-like differentiation: its specific expression in the smooth muscle cell tumor. Hum Pathol. 1999;30:392-396.
[36.] Miettinen MM, Sarlomo-Rikala M, Kovatich AJ, Lasota J. Calponin and h-caldesmon in soft tissue tumors: consistent h-caldesmon immunoreactivity in gastrointestinal stromal tumors indicates traits of smooth muscle differentiation. Mod Pathol. 1999;12:756-762.
Accepted for publication October 19, 2000.
From the Pathology Division, Fukushima Medical University School of Medicine Hospital, Fukushima, Japan (Drs Watanabe and T. Suzuki); and the Divisions of Pathology (Dr Saito) and Otolaryngology (Drs M. Suzuki and Yamanobe), Jusendo General Hospital, Koriyama, Japan.
Reprints: Kazuo Watanabe, MD, Pathology Division, Fukushima Medical University School of Medicine Hospital, 1 Hikariga-oka, Fukushima City, 960-1295, Japan (e-mail: email@example.com).
|Printer friendly Cite/link Email Feedback|
|Author:||Watanabe, Kazuo; Saito, Atsuko; Suzuki, Masahiro; Yamanobe, Shu; Suzuki, Toshimitsu|
|Publication:||Archives of Pathology & Laboratory Medicine|
|Date:||May 1, 2001|
|Previous Article:||Bilateral Renal Oncocytosis With Renal Failure.|
|Next Article:||Retroperitoneal Mucinous Cystadenoma: Report of a Case With Reference to Histogenesis.|