Abstract
Background
The surgical ciliated cyst of the maxilla was initially reported as a sequela of Caldwell–Luc type open maxillary sinus procedures. Recently, other etiologies have become apparent and cases have been reported outside of the maxilla. They have the potential for local destruction and at times may mimic a locally aggressive tumor or cyst. We aim to elucidate the etiopathogenesis of the surgical ciliated cyst to improve prevention, diagnosis and treatment of these lesions.
Body
A systematic review of the literature using PubMed and Scopus databases was conducted to assess the presentation, treatment, and outcomes of this disease. Surgical ciliated cysts of the maxillofacial region shows a 1.1:1 female-to-male ratio with a protracted time to diagnosis (range: 4–22 years). Typically, radiology shows a unilocular radiolucency (95%) and histology predominantly shows pseudostratified ciliated columnar epithelium (58%). The most common treatment of these lesions involves enucleation and curettage. In rare instances, transfacial approaches, resection, and reconstruction are required. Recurrence ranges from 6 to 20%.
Conclusion
Surgical ciliated cyst should be considered in a patient presenting with an orofacial mass or edema who has a history of maxillofacial injury or surgery. Timely diagnosis will decrease the severity and morbidity associated with this entity. Meticulous surgical technique can aid in the prevention of this lesion.
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Background
The postoperative maxillary cyst (POMC) was first reported in the literature by Kubo et al. (1927). Unaware of the lesion’s prior description, Gregory and Shafer reported three cases in 1958 as “surgical ciliated cyst of the maxilla (SCCM).” (Gregory and Shafer 1958) Further publications ensued, initially mostly in the Japanese literature (Kubo and Shida 1961; Mizutani et al. 1974; Mohri et al. 1977; Odawara 1965; Sato et al. 1969; Hashimoto et al. 1987; Nakamura et al. , 1075; Fukuta et al. 1987; Kaneko et al. 1989; Sawano et al. 2005; Yamada et al. 1991; Shik 1989; Yang et al. 2018; Kuroishikawa 2000; Yu and Lin 1998; Toda et al. 1990). However, it is now well documented across geographical regions (Coviello et al. 2016; Koo Min Chee et al. 2014; Moe et al. 2013; Kaneshiro et al. 1981; Yoshikawa et al. 1982; Yamamoto and Takagi 1986; Basu et al. 1988; Miller et al. 1988; Sugar et al. 1990; Misch et al. 1991; Hayhurst et al. 1993; Hasegawa and Kuroishikawa 1993; Nastri and Hookey 1994; Józefowicz-Korczyńska and Latkowski 1995; Lockhart et al. 2000; Imholte and Schwartz 2001; Yoshizaki and Watanabe 2002; Koutlas et al. 2002; Amin et al. 2003; Lazar et al. 2003; Bartnik and Bartnik-Krystalska 2004; Bourgeois and Nelson 2005; Shakib et al. 2009; Cano et al. 2009; Ragsdale et al. 2009; Bulut et al. 2010; Leung et al. 2012; Kim et al. 2013; Fernandes et al. 2013; Lee et al. 2014; An and Zhang 2014; Li et al. 2014; Toyoshima et al. 2014; Cai et al. 2015; Adachi et al. 2016; Niederquell et al. 2016; Yamamoto et al. 2017; Martinelli-Kläy et al. 2017; Matsuzaki et al. 2017; Han 2018; Tanio et al. 2019; Golaszewski et al. 2019; Siwach et al. 2020; Pe et al. 1990; Kondo et al. 2018; Heo et al. 2000; Gang et al. 2014; Yamaura et al. 2005).
The traditionally accepted pathogenesis of SCCMR involves entrapment of nasal or maxillary sinus mucosa, a subsequent inciting inflammatory process, and progressively increased osmotic pressure. Together, these steps lead to cyst creation, expansion, and enlargement. Early publications detailed this event occurring most often as a sequelae of open maxillary sinus surgery (Kubo and Shida 1961; Mizutani et al. 1974; Mohri et al. 1977; Odawara 1965; Sato et al. 1969; Hashimoto et al. 1987; Nakamura et al. , 1075; Fukuta et al. 1987; Kaneko et al. 1989; Sawano et al. 2005; Yamada et al. 1991; Shik 1989; Yang et al. 2018; Kuroishikawa 2000; Yu and Lin 1998; Toda et al. 1990). The advent of functional endoscopic sinus surgery has decreased the incidence of this etiology. However, the entrapment of nasal or sinus mucosa within a facial fracture or osteotomy line remains a common cause. As such, the etiology of surgical ciliated cysts has evolved to include: The transplantation of respiratory mucosa to the mandible during combined rhinoplasty/genioplasty, contamination of surgical instruments in double jaw surgery, and the improper management of nasal or sinus mucosal perforation in dental implant surgery. This has led to the discovery of surgical ciliated cysts outside of the maxilla (Kubo 1927; Sawano et al. 2005; Yu and Lin 1998; Hayhurst et al. 1993; Yoshizaki and Watanabe 2002).
The clinical presentation depends upon the location of cyst formation, direction of growth, size, and amount of bone loss or resorption. It may present as a palpable swelling or mass in the mucobuccal fold of the maxilla or mandible, the palate, naso-orbital region, or midface. Extragnathic presenting symptoms may include facial deformity, nasal obstruction, orbital proptosis, or visual changes. As it can be found anywhere within the facial skeleton, the name surgical ciliated cyst of the maxillofacial region (SCCMR) seems more inclusive.
The incidence of the SCCMR is not well known. Basu et al. reported an incidence of SCCMR of approximately 1.5% of all oral cysts encountered in their institution’s pathology registry. Their publication provides great detail in the classic findings of SCCMR and how to distinguish it from other entities on a histopathologic and microbiologic basis (Yu and Lin 1998).
To better understand and characterize this often unrecognized entity, we have undertaken a systematic review of SCCMR.
Materials and methods
A systematic review of the literature was conducted using the Preferred Reporting Items for Systematic Review and Meta-Analysis (PRISMA) method (Moher et al. 2009). Our intent was to search the literature for all patient-related cases of SCCMR. PubMed (MEDLINE) and Scopus were queried using the following terms: “surgical ciliated cyst” OR “postoperative maxillary cyst” OR “surgical implantation cyst” or “respiratory implantation cyst.” All results from inception of the registry to August 18, 2020, were included.
Articles were screened by the first author J.C.G. and results reviewed independently by authors J.C.G and E.C. Any discrepancies were reviewed and settled with verbal discussion. Studies were included for review if the (a) title and abstract included the desired search terms; (b) abstract contained patient-related data; (c) abstract was equivocal, full article review revealed patient case(s).
Articles were excluded if (a) the article reported on a different type of cyst, neoplasm or disease; (b) there was redundant reporting of clinical cases; (c) the article described only the surgical treatment of the cyst or related lesion without patient data; (c) the article only described the histopathology of the disease; (d) the article type was a letter to the editor, book chapter, opinion, or poster; (e) both the abstract and article were not available.
After completion of the abstract review, the references for included publications were screened and cross checked for any additional studies that met inclusion criteria. A total of 50 publications were included (Fig. 1).
Clinical information was compiled into tables in Microsoft Word including: total number of cases, age, gender, etiology, duration from inciting factor to diagnosis, clinical, radiologic, and histologic findings, and treatment. A summary of the data is presented (Tables 1, 2) and the details are presented as Additional file 1: Appendix 1–4.
Results
Fifty publications and 205 cases of surgical ciliated cyst were included. They were all retrospective, level 4 evidence. One hundred of the cases included gender information, with a 1.1:1 female-to-male ratio. Ninety-eight cases provided definitive etiology regarding the cause of the SCCMR (Table 1). In some case series, the etiologies were listed but not matched to patient presentation or treatment and were therefore left out, leaving only approximately one half of the publications for analysis. Only two cases were presented as being spontaneous in nature with an incidence of 1% and we believe these to be likely from unrecognized inciting event.
In our review, the predominant clinical presenting features are: mucobuccal and facial edema following Caldwell Luc type procedures; palatal, mucobuccal or mandibular swelling from orthognathics (Fig. 2A); facial or orbital edema with potential for nasal or visual disturbance from trauma; or maxillary or mandibular mucobuccal fold edema from sinus lift and dental procedures (Kuroishikawa 2000). The latency period (Table 1) in our analysis was calculated as the interval from inciting traumatic event or surgery to diagnosis.
A Example of a clinical presentation of a surgical ciliated cyst in a 41-year-old female with painful, infected palatal mass like edema ten years post-Le Fort 1 maxillary orthognathic surgery. B Radiologic correlate in this axial bone window of a CT facial bones scan shows typical radiologic findings of surgical ciliated cyst: expansile unilocular radiolucent lesion which originates from maxillary fixation screws and plate
The most common radiologic presentation was that of a homogenous, corticated, unilocular radiolucency (95.5%), with cortical perforation occurring 23% of the time (Fig. 2B).
SCCMR is by definition characterized by respiratory epithelium (Figs. 3, 4). All SCCMR is therefore pseudostratified ciliated columnar epithelium and the only relevant histologic findings are the presence or absence of metaplasia within the cyst. When provided, we found a predominance of respiratory type epithelium alone (58%) with cuboidal and squamous metaplasia occurring less frequently (36%).
Several studies presented case matched details on treatment rendered (Table 2 and Additional file 1: Appendix 5). Enucleation and curettage alone was the most commonly employed treatment (56%).
Discussion
SCCMR is a destructive, postsurgical, or post-traumatic lesion which may mimic other cysts and tumors of the maxillofacial region, given its ability to cause bone and hard tissue loss. It should be suspected in someone with prior craniomaxillofacial surgery, or trauma, presenting with mass-like edema or pain, or a radiolucent lesion in the site of prior surgery. The latency time can be very long, spanning up to several decades from inciting events to clinical presentation. The predominant histologic finding in our review is that of pseudostratified ciliated columnar epithelium. Other, less common pathologic findings include squamous and cuboidal metaplasia with goblet cells.
Severe cases often exhibit extensive local bone loss, cortical perforation, fistula formation, or extension into nearby anatomic structures such as the maxillary sinus, nasal cavity, orbit, and adjacent facial bones (Kuroishikawa 2000; Józefowicz-Korczyńska and Latkowski 1995; Bartnik and Bartnik-Krystalska 2004; Leung et al. 2012; Golaszewski et al. 2019; Kusunoki and Ikeda 2012). This is corroborated by others who note that their initial clinical suspicion was of a more destructive or even malignant lesion (Józefowicz-Korczyńska and Latkowski 1995; Bartnik and Bartnik-Krystalska 2004). Kusunoki et al. describe a large maxillary sinus lesion they presumed to be a SCCMR due to the extent of maxillary bone loss, yet upon histologic examination, it was found to be neuroendocrine carcinoma (Kusunoki and Ikeda 2012).
Time to diagnosis for these patients was found to be a mean range of five to 22 years depending upon etiology (Table 1). This is consistent with another recent review by Golaszewski et al., which showed a 15.83-year average latency time (Golaszewski et al. 2019). Fernandes et al. published a case report in 2013 that exemplifies the nuances in the diagnosis of SCCMR. In their publication, the patient developed symptoms five years after surgery and endured 10 years of unsuccessful multiple incision and drainage procedures as well as medical treatment with antibiotics. The diagnosis was finally made 15 years later, when the lesion had grown and caused significant bone loss (Fernandes et al. 2013).
An initial treatment algorithm was proposed by Yoshikawa et al. which included: enucleation and curettage alone, enucleation with primary closure, marsupialization, or open packing (Yoshikawa et al. 1982). Other treatments have been described since this early publication including: irrigation and curettage (Sawano et al. 2005; Koutlas et al. 2002), Le Fort 1 down fracture for access (Hayhurst et al. 1993), transfacial approach via lateral rhinotomy for en bloc resection (Adachi et al. 2016), and endoscopic sinus surgery (Yang et al. 2018). The authors believe that prompt surgical treatment of this disease should be completed upon its recognition. Treatment goals should include the removal of the entire cystic lining, in an en bloc fashion if possible. With this in mind, curettage and ostectomy with a surgical handpiece should be employed as adjuvant measures to ensure all epithelial remnants are removed. In addition, any hardware or foreign body that may have caused mucosal entrapment should be removed to treat the source of the cyst. Access for the surgery may be possible in transoral fashion for most cases; however, some may require trans-facial approach. The surgeon may also consider an endoscopic approach as long as it does not prohibit en bloc removal of the cyst, curettage, ostectomy, and hardware removal. Recurrence is thought to occur with incomplete removal of the cyst lining and is reported to range from 6 to 20% (Yoshikawa et al. 1982; Li et al. 2014; Lee and Lee 2010). More specifically, Yoshikawa et al. reported seven recurrences out of 110 cases; however, they did not correlate to treatment rendered (Yoshikawa et al. 1982). Finally, any delay in surgical treatment for conservative therapies such as marsupialization, packing, irrigation, injection, or aspiration will only delay the diagnosis and time to definitive surgical treatment. This may incur increased morbidity to the patient.
Prevention of SCCMR may be possible with meticulous surgical technique, including: suturing torn nasal mucosa (Hayhurst et al. 1993); removing/stripping sinus mucosa during orthognathic or facial trauma procedures (Kühnel and Reichert 2015); cleaning/changing the saw blades after maxillary osteotomy (Bourgeois and Nelson 2005); close inspection and thorough irrigation of osteotomies to flush entrapped mucosa (Bourgeois and Nelson 2005); doing mandible surgery first (Bourgeois and Nelson 2005); abstaining from the use of residual maxillary or nasal bone autograft for use in the mandible or any other sites (Cai et al. 2015); preventing mucosal impaction in fractured segments (An and Zhang 2014); and meticulous maintenance of the Schneiderian membrane in sinus lift (Yamamoto and Takagi 1986).
While our review is the largest attempt to characterize and provide both preventative, diagnostic, and treatment recommendations for SCCMR, it has limitations. First, there are many articles in other languages or older texts that were not obtainable. This presents a reporting bias. Second, not every case report or series was reported uniformly. Therefore, some cases are missing demographic or clinical information. Third, this data is all presented retrospective fashion which may lead to selection bias of only cases reported that were significant or notable. Finally, the larger case series reported their findings as cohorts, whereas case reports and case series reported specific case details for each patient (Kaneshiro et al. 1981; Basu et al. 1988). This made it difficult to pool data regarding etiology from the case reports with the data from the larger case series.
Conclusions
Consideration of SCCMR in the differential diagnosis of a patient with prior maxillofacial injury or surgery presenting with orofacial mass, edema, or incidental radiolucency is important. Prompt recognition and consideration in the differential diagnosis will aid in decreasing the time to diagnosis, morbidity, and severity of these lesions. Treatment via enucleation and curettage with source control should be completed upon diagnosis, though more aggressive measures may be needed. This article should also serve to remind practitioners of the ways in which meticulous surgical technique can aid in the prevention of the formation of this lesion altogether.
Availability of data and materials
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Abbreviations
- SCCMR:
-
Surgical ciliated cyst of the maxillofacial region
- POMC:
-
Postoperative maxillary cyst
- SCCM:
-
Surgical ciliated cyst of the maxilla
- PRISMA:
-
Preferred reporting items for systematic review and meta-analysis
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LG worked on conceptualization, composition of manuscript, and final approval. DT worked on methodology and final approval. JG worked on conceptualization, composition of manuscript, methodology, literature search, and final approval. MT worked on conceptualization and final approval. EC worked on literature search, composition of manuscript, and final approval. All authors have read and approved the manuscript.
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Additional file 1.
Appendices. Appendix 1. Surgical Ciliated Cyst of the Maxillofacial Region Demographics. Appendix 2. Clinical Presentation of SCCMR Systematic Review. N= number of patients, NA = not available. Appendix 3. Radiologic Presentation of SCCMR. Appendix 4. Histologic Presentation of SCCMR. Appendix 5. SCCMR Treatment.
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Gates, J.C., Taub, D.I., Cherkas, E. et al. Surgical ciliated cyst of the maxillofacial region: a systematic review. Bull Natl Res Cent 46, 235 (2022). https://doi.org/10.1186/s42269-022-00925-7
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DOI: https://doi.org/10.1186/s42269-022-00925-7