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Head Neck Pathol. 2007 September; 1(1): 38–43.
Published online 2007 November 28. doi:  10.1007/s12105-007-0025-2
PMCID: PMC2807499

Update on Sinonasal Adenocarcinoma: Classification and Advances in Immunophenotype and Molecular Genetic Make-Up

Introduction

Adenocarcinomas of various types comprise 10% to 20% of all primary malignant neoplasms of the nasal cavity and paranasal sinuses [1].

Salivary Gland-Type Adenocarcinomas

Adenocarcinomas of salivary-gland type are uncommon constituting 5–10% of sinonasal adenocarcinomas. They are thought to originate from seromucus glands of the nasal cavity and paranasal sinuses as well as the surface epithelium. Histologically, these carcinomas are similar to those originating from major and minor salivary glands [2]. The most common type is adenoid cystic carcinoma (Fig. 1) usually occurring in the maxillary sinus and nasal cavity [3]. Long-term prognosis is poor and patients usually die due to local spread with no metastasis. Adenocarcinoma Not Otherwise Specified may exhibit many high-grade, poorly differentiated growth patterns, and should be considered as a diagnostic entity for many high-grade salivary gland-type adenocarcinomas of the sinonasal tract. These tumors have a poor prognosis [1, 4].

Fig. 1
Adenoid cystic carcinoma of nasal cavity. Classic cribriform and cystic pattern with bland nuclear appearance. Nasal surface epithelium is at the top left corner. H-E-stain x250

Other types of salivary adenocarcinomas are rare in the sinonasal tract but cases of acinic cell carcinoma, mucoepidermoid carcinoma (Fig. 2) [5], epithelial-myoepithelial carcinoma, basal cell adenocarcinoma, salivary duct carcinoma, polymorphous low-grade adenocarcinoma (terminal tubulus adenocarcinoma) [6], and carcinoma-ex-pleomorphic adenoma have been reported. The possibility of specific types of salivary gland-type adenocarcinomas should be taken into account when considering the diagnosis of a sinonasal adenocarcinoma. Table 1 lists the occurrence of different types of salivary gland-type tumors in the sinonasal tract.

Fig. 2
Low-grade mucoepidermoid carcinoma of nasal cavity. Islands of intermediate cells contain mucous cysts and few epidermoid cells. Nasal surface epithelium at left. H-E stain x250
Table 1
Occurrence of sinonasal tumors of salivary gland type (modified from reference #5)

Non-Salivary Gland-Type Adenocarcinomas

The WHO classification of non-salivary gland-type adenocarcinomas [7] follows a classical distinction into intestinal-type adenocarcinoma and non-intestinal-type adenocarcinoma. WHO further subdivides the latter into low-grade and high-grade carcinoma [7]. Another approach first pools the various types of non-salivary gland-type sinonasal adenocarcinomas together and distinguishes them into six histological groups: low-grade, papillary, colonic, solid, mucinous, and mixed types [8]. In this presentation, the WHO classification of 2005 is used.

Intestinal-Type Sinonasal Adenocarcinoma

General

After adenoid cystic carcinoma, intestinal-type sinonasal adenocarcinoma is the second most common type of adenocarcinoma of the sinonasal tract. These carcinomas mimic the appearance intestinal adenomas and carcinomas, or exceptionally the normal glandular epithelium of the intestinal mucosa. The most commonly involved site is the ethmoid sinus (40%), followed by the nasal cavity (25%) and the maxillary antrum (20%). In advanced cases, local spread often occurs to the orbit, the pterygopalatine and infratemporal fossae, and into the cranial cavity.

The presenting symptoms include nasal obstruction and epistaxis. Most patients are male (male-female ratio is around 4:1) and there is a wide age range at presentation.

Nasal cavity adenocarcinoma of a non-salivary type was first recognized by Citelli and Calamida in 1903. Cell types and growth patterns of these tumors were characterized later by Masson and Martin in 1928, Ringertz in 1938, and Jarvi in 1944.

Major interest for the intestinal-type sinonasal adenocarcinoma was first stimulated by the discovery of its link to long-term exposure to hardwood dusts in British woodworkers [9]. Since then, the association of occupational exposure to hardwood (beech, oak) and leather dusts and intestinal-type sinonasal adenocarcinomas has been firmly established [1012]. Also, occupational exposure to softwood dusts, textile dusts, paints, varnishes, lacquers, glues, and adhesives has been incriminated [13, 14]. Reportedly, exposure to softwood dusts (pine, fir) could also associate with sinonasal squamous cell carcinoma [15]. In woodworking industry the incidence of sinonasal carcinoma may be 1,000 times that of the population in general [16]. Approximately one in five cases of sinonasal intestinal-type adenocarcinoma has been traced to wood-dust exposure in woodworking industry. An average exposure time of 40–43 years has been reported [1]. Cases related to industrial wood-dust exposure show a strong predilection for the ethmoid sinus, while sporadic tumor cases are often seen in the maxillary antrum.

Histopathology

Histopathology of these adenocarcinomas recapitulates the range of appearances of neoplastic and normal large and small intestinal mucosa [17]. Classification of these tumors according to Barnes includes five patterns: colonic, papillary, solid, mucinous and mixed [1]. Alternatively, the classification of Kleinsasser and Schroeder comprises four types: papillary tubular cylinder cell of various grades, alveolar goblet type, signet-ring type, and transitional type [13].

Reportedly, the most common forms of intestinal-type sinonasal adenocarcinoma resemble colonic adenocarcinoma. In the colonic type, a predominantly tubulo-glandular architecture with some papillary elements is seen. The glandular neoplastic cells of these tumors have palisaded hyperchromatic nuclei and a few goblet cells. In the papillary type, growth pattern is predominantly papillary with tubular elements (Fig. 3). In the solid type, tumor is poorly differentiated and the glandular architecture is gradually lost and replaced by a trabecular and solid proliferation. In analogy to colonic adenocarcinomas, some tumors exhibit predominantly mucinous features. In such cases, neoplastic glands tend to be distended with mucin, or clusters of tumor cells are found within pools of mucin that extend into connective tissue stroma (Fig. 4). Often, small numbers of signet-ring cells can be identified in these tumors. The mixed type is composed of two or more of the previous patterns in variable mixtures. In all histologic types, specialized cell types such as goblet cells, resorptive cells, Paneth cells, and argentaffin cells may be encountered.

Fig. 3
(A) Intestinal-type adenocarcinoma, papillary growth pattern. The papillary elements contain tubular and glandular structures of various types. Invasive growth to stroma is seen. H-E-stain x 250. (B) Tumor of Fig. 3A. The nuclei are often hyperchromatic ...
Fig. 4
Intestinal-type adenocarcinoma, mucinous growth pattern. Alveolar pattern of groups of neoplastic cells containing goblet-type cells, and suspended in a pool of mucin. In another area of this tumor, poorly differentiated papillae of intestinal type containing ...

Exceptional well-differentiated intestinal-type sinonasal adenocarcinomas may closely resemble normal small intestinal mucosa (Fig. 5). Well-formed villi and a muscularis mucosae can be present. These lesions may look deceptively like benign heterotopias, but they are aggressive and invasive in nature [18].

Fig. 5
(A) Low-grade non-intestinal adenocarcinoma. A complex papillary growth pattern with tubular and glandular structures. A single layer of bland columnar cells line the papillae. H-E stain x160. (B) Another low-grade non-intestinal adenocarcinoma. A single ...

Differential Diagnosis

Sinonasal adenocarcinomas with an appearance of conventional or mucinous colonic adenocarcinoma should be examined with a second thought of a possible metastatic lesion from the gastrointestinal tract. In accordance to colonic adenocarcinomas, intestinal-type sinonasal adenocarcinomas stain for CK20, CDX-2, MUC2, but in contrast to colonic adenocarcinomas also for CK7 [19, 20]. Intestinal-type sinonasal adenocarcinomas often stain for chromogranin while staining for CEA is variable [21]. However, so far the differentiation of primary sinonasal tumors of the intestinal type from the rare possibility of a metastatic lesion using immunohistochemical markers or morphologic features remains uncertain [19, 22]. Molecular genetic studies of intestinal-type sinonasal adenocarcinomas indicate frequent mutations in K-RAS [23] and TP53 [24, 25]. In cases with occupational dust exposure, intestinal-type sinonasal adenocarcinomas showed a deregulation of p16(INK4a) associated with that of TP53 or p14(ARF) [25]. The gatekeeper events of their early development (p16(INK4a) and TP53) seem to differ from colorectal adenocarcinomas (APC) [24].

When considering the differential diagnostic possibility of a metastatic lesion, one should remember that among metastatic lesions to the sinonasal tract, primary tumors in the gastrointestinal tract are unusual [1, 4].

However, if the microscopic appearance of a sinonasal carcinoma resembles that of a colorectal carcinoma, colonoscopy is a straightforward and recommended approach. The rare intestinal-type sinonasal adenocarcinomas that have an appearance reminiscent of normal intestinal mucosa and those resembling a villous adenoma are always nasal in origin, and should pose no differential diagnostic problems.

The differential diagnosis of intestinal-type sinonasal adenocarcinomas may include low-grade sinonasal adenocarcinoma [20, 22] or sometimes non-neoplastic papillary sinusitis with abundant mucinous material.

Treatment and Prognosis

The treatment of intestinal-type sinonasal adenocarcinoma is adequate surgical removal, and in advances cases this is combined with postoperative radiotherapy. Surgical procedures include lateral rhinotomy combined with partial maxillectomy and ethmoidectomy according to spread of the tumor. In advances cases, radical maxillectomy may be indicated. Chemotherapy seems to be of uncertain benefit.

Intestinal-type sinonasal adenocarcinomas behave as high-grade aggressive malignancies. In reviewed materials [1, 17], half of patients experienced local recurrence, and locoregional and/or distant metastasis was seen in 10–20% of cases. Up to two thirds of patients died of disease, usually due to local spread to vital structures. It was reported that cases related to industrial dust exposure had a 50% survival at 5 years, while sporadic tumors showed a 20–40% 5-year survival [1]. In another material, however, no survival difference between cases with occupational exposure and sporadic cases was found [17].

Most patients have an advanced disease at presentation, and clinical staging is usually not informative of prognosis. However, the histologic subtype has prognostic significance for clinical behaviour [1, 13, 17]. The papillary subtype has been associated with an 80% survival at 5 years, while the mucinous and solid subtypes carry a poor prognosis. H-RAS mutation and certain immunophenotypes may also associate with behaviour [26].

Non-Intestinal-Type Sinonasal Adenocarcinomas

These adenocarcinomas apparently arise from the surface epithelium of the sinonasal tract. They do not share microscopic appearances with salivary gland-type sinonasal adenocarcinomas or intestinal-type sinonasal adenocarcinomas. According to WHO [17] they are divided into low- and high-grade types.

Non-salivary-type Low-grade Adenocarcinoma

General

Low-grade sinonasal adenocarcinomas occur in a wide age range with a mean age of 37–53 years at presentation. Most frequently involved sites are the ethmoid sinus, the nasal cavity, and the maxillary sinuses [4]. Association with occupational or environmental carcinogens has not been reported in these tumors.

Histopathology

Non-salivary-type (and non-intestinal-type) sinonasal low-grade adenocarcinomas are a distinctive group of tumors with mostly papillary and glandular appearance [7]. Other patterns include trabecular, cribriform, clear cell [27], and mucinous. In non-intestinal-type sinonasal adenocarcinomas, papillae and small glands are lined by a single layer of uniform cells (Fig. 5), or less frequently by a double layer containing also basal/myoepithelial cells. Neoplastic glands may have a back-to-back arrangement without intervening stroma. The glands may also contain well-formed papillae, be cystically dilated, and contain mucin. Nuclei tend to be round and uniform in size with inconspicuous nucleoli. Mitotic figures are rare, and no atypical mitoses and necrosis are seen. The appearance of these neoplasms is bland but the complexity of their pattern and local invasive growth indicate malignancy. A tubulopapillary variant (Fig. 6) that may simulate terminal tubulus adenocarcinoma of the nasal seromucus glands, has been discussed recently [2830].

Fig. 6
(A) Tubulopapillary low-grade (non-intestinal) adenocarcinoma. A papillary growth pattern with tubular and trabecular formations in the stroma. A single layer of cuboidal to columnar cells with round uniform nuclei, indistinct nucleoli and eosinophilic ...

Tumors with similar appearances termed nasopharyngeal papillary adenocarcinomas may originate in the nasopharynx and may extend into the nasal cavity [31]. In these tumors, the papillae are arborized and have fibrovascular cores. The epithelial cells are columnar or pseudostratified. Moderate nuclear pleomorphism may be encountered but mitoses are infrequent [31].

Differential Diagnosis

The most important differential diagnosis of low-grade sinonasal adenocarcinoma is intestinal-type sinonasal adenocarcinoma. Low-grade sinonasal adenocarcinomas have been reported to lack intestine-specific immunophenotypic markers such as CDX-2, MUC-2, and CK20 [22]. In intestinal-type adenocarcinomas, the intestinal appearance and a distinct intestine-specific immunophenotype [22] facilitate distinction. Intestinal-type adenocarcinomas also show more cytologic pleomorphism, except in rare cases where the nasal neoplasm closely resembles normal intestinal mucosa. Low-grade sinonasal adenocarcinomas may sometimes be difficult to differentiate from oncocytic Schneiderian papillomas or metastatic papillary carcinoma of the thyroid [4].

Treatment and Prognosis

The treatment of low-grade sinonasal adenocarcinoma is complete surgical excision. These tumors are mostly localized at presentation, and the required surgery usually is not extensive. In cases of extensive disease or higher-grade lesions, radiotherapy may be utilized. Local recurrences have been reported in some cases, and death of disease has occurred due to local invasion [4]. However, low-grade sinonasal adenocarcinoma has a favourable overall prognosis.

References

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