Primary combined small and squamous cell carcinoma of the hypopharynx: A case report
Affiliations: Department of Otolaryngology/Head and Neck Surgery, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka 431‑3192, Japan, Department of Regenerative and Infectious Pathology, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka 431‑3192, Japan, Second Department of Surgery, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka 431‑3192, Japan, Department of Otolaryngology/Head and Neck Surgery, Jichi Medical University, Shimotsuke, Tochigi 329‑0498, Japan
- Published online on: February 22, 2016 https://doi.org/10.3892/mco.2016.788
- Pages: 709-714
Copyright: © Misawa et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
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Primary malignant tumors of the hypopharynx are predominantly squamous cell carcinomas (SqCCs), as primary small-cell carcinoma (SmCC) of the hypopharynx is rare. Combined primary SmCC and SqCC of the hypopharynx, referred to as composite tumor of the hypopharynx, is even more rare, with only 3 cases previously reported (1–3). Therefore, there is little information available on the optimal management of these patients. We herein report a the case of a patient with primary combined SmCC with an SqCC element and investigate the expression of specific proteins for molecular-targeted therapy.
A 74-year-old man, with a ~50-year history of excessive alcohol consumption and smoking, presented with a 3-month history of throat pain and hoarseness. There was no history of weight loss, dysphagia, or dyspnea. On hypopharyngoscopy, a tumor was identified in the right anterior wall of the piriform sinus (Fig. 1A). A pathologist analyzed the biopsy sample and diagnosed the lesion as SqCC, as no SmCC component was identified in the biopsy specimen. The right vocal cord was not fixed. A contrast computed tomography (CT) scan of the neck revealed a heterogeneously enhanced tumor sized 25×17×38 mm extending through the right piriform sinus (Fig. 1B). Moreover, fluorodeoxyglucose positron emission tomography (FDG-PET) revealed high-level accumulation in the primary tumor, with a maximum standardized uptake value of 14.6. There was no evidence of cervical lymph node metastasis, primary lung tumor, or distant metastasis. The patient was diagnosed with hypopharyngeal cancer classified as T2N0M0, according to the 2009 Union for International Cancer Control staging system (4). We performed a tracheostomy, total laryngectomy, right hemithyroidectomy and bilateral lateral neck dissection (level II–IV). The macroscopic surgical specimen is presented in Fig. 1C. The specimen consisted of the resected larynx and right piriform sinus tumor. A 25×20-mm deeply ulcerated tumor was found in the right piriform sinus. Microscopically, two components were identified in the lesion, namely a poorly differentiated SqCC and an SmCC containing chromatin-rich nuclei with scanty cytoplasm (Fig. 2A). Pathologically, multiple metastatic cervical lymph nodes were identifed bilaterally (right side, levels II and III; and left side, level III). Although the surgical margin was narrow, it was negative for cancer cells.
(A) Hypopharyngeal fiberscopic image. An ulcerated tumor was identified in the right piriform sinus. (B) Contrast computed tomography scan of the neck prior to treatment. An enhanced tumor was identified in the right piriform sinus. (C) Macroscopic surgical specimen. A deeply ulcerated tumor is seen in the right piriform sinus (arrow).
Microscopic images of the surgical specimen. (A) Hematoxylin and eosin staining. This tumor consisted of a combination of small-cell carcinoma (SmCC) and squamous cell carcinoma (SqCC). (B) Collision phase showing invasive SqCC in gradual transition with adjacent SmCC. (C) SmCC component (arrow) infiltrating a lymphatic vessel. (D) Metastatic lymph nodes mainly involved the SmCC component (arrows). (E) CD56 was expressed in the SmCC component. (F) The SmCC component of the neck lymph node was positive for CD56. (G) The SmCC component was negative for cytokeratin (CK) 34βE12. (H) The SqCC component was positive for CK 34βE12. (I) Staining of the SmCC component revealed a high Ki-67 labeling index of 50.2%. (J) The Ki-67 labeling index was 47.5% in the SqCC component.
Concomitant chemoradiotherapy (cisplatin + etoposide with 45 Gy) was administered postoperatively. However, after the first course, adjuvant chemotherapy was discontinued due to prolonged bone marrow suppression, although the therapy was effective. However, despite treatment, distant metastases in the thoracic vertebrae (T5, 9 and 10) were confirmed by CT 6 months later. The patient's condition started to deteriorate and he succumbed to the disease 7 months after the initial treatment.
On gross examination of the laryngectomy specimen, a mass involving the right piriform sinus was palpable. The tumor extended superiorly to involve the right supraglottis and exhibited variable gross morphology, ranging from ulcerated, to nodular, to plaque-like growth. The tumor infiltrated 1.3 cm in depth, but did not involve the thyroid cartilage, vocal cord, or trachea. Microscopic sections from the larynx revealed a combined tumor, composed predominantly of SmCC localized in the upper side and SqCC localized in the lower side (Figs. 1 and 2A). We observed 2 components in the lesion: A poorly differentiated SqCC and a small-sized SmCC with finely granular, hyperchromatic nuclei, inconspicuous nucleoli and scanty cytoplasm. There was a transitional area between the SmCC and SqCC (Fig. 2A and B). The metastatic potential of the lesion was further supported by the SmCC component found to infiltrate lymphatic vessels (Fig. 2C). The metastatic lymph nodes primarily involved the SmCC component (Fig. 2D).
Immunohistochemically, the SmCC strongly expressed CD56 (Fig. 2E) and cytokeratin (CK) AE1/AE3. Diffuse CD56 positivity in the SmCC component in the cervical lymph nodes supported the histological diagnosis (Fig. 2F). The SmCC component was also negative for CK 34βE12 (Fig. 2G), p63, synaptophysin, chromogranin A and CD45. The SqCC component was negative for neuroendocrine markers, including CD56, synaptophysin and chromogranin A, although it was positive for CK 34βE12 (Fig. 2H). Immunoreactivity to Ki-67 was seen in the nuclei of tumor cells. In the SmCC component, the Ki-67 labeling index was 50.2%, while that in the SqCC component was 47.5% (Fig. 2I and J).
To predict the prognosis of this patient, we evaluated the expression of epidermal growth factor receptor (EGFR). Furthermore, to evaluate the possibility of using molecular-targeted therapy for combined SmCC and SqCC, the expression of proteins such as platelet-derived growth factor receptor α (PDGFRα), vascular endothelial growth factor receptor 2 (VEGFR2) and KIT was examined. On immunohistochemical analysis, the SmCC element was strongly positive for KIT and PDGFRα; however, EGFR and VEGFR2 were not expressed (Fig. 3A, C and E). The SqCC element was mildly positive for PDGFRα and EGFR; however, KIT and VEGFR2 were not expressed (Fig. 3B, D and F).
(A) KIT was expressed in the small-cell carcinoma (SmCC) component, but (B) not in the squamous cell carcinoma (SqCC) component. (C) The SmCC component was negative for epidermal growth factor receptor (EGFR), but (D) the SqCC component was positive for EGFR. (E and F) Immunostaining demonstrated that both components were positive for platelet-derived growth factor receptor α (PDGFRα).
DNA extraction, genetic analysis and human papillomavirus (HPV) polymerase chain reaction
DNA was isolated from the SmCC element in specimens obtained during surgery. Genomic DNA was extracted from frozen tumor specimens using the QIAamp DNA Mini Kit (Qiagen, Hilden, Germany), according to the manufacturer's protocol.
A molecular genetic analysis of KIT (exons 9, 11, 13 and 17) and PDGFRα (exons 12, 14 and 18) was performed using the polymerase chain reaction (PCR) direct sequencing method, as previously reported (5–8). PCR products were extracted and subjected to a computed automatic DNA sequencing (ABI PRISM 3100 Genetic Analyzer; Applied Biosystems, Carlsbad, CA, USA). This case exhibited a silent mutation in exon 12 of PDGFRα (Fig. 4); we observed an A→G change in codon 567 (CCA→CCG). Analysis of exon 12 of PDGFRα from other normal tonsillar tissues revealed a similar A→G change at the 1849 nucleotide position. Comparison of this sequence variation with the single-nucleotide polymorphism (SNP) database revealed the presence of a known SNP at codon 567 of PDGFRα (9).
Electropherogram with relative sequence for the small-cell carcinoma elements of exon 12 of the platelet-derived growth factor receptor α gene.
The HPV status was determined using the HPV Typing Set (Takara Bio., Tokyo, Japan), a PCR primer set specifically designed to identify HPV genotypes 16, 18, 31, 33, 35, 52 and 58 in genomic DNA. The PCR HPV Typing Set method was used according to the manufacturer's protocol. The PCR products were separated by electrophoresis through a 9% polyacrylamide gel and stained with ethidium bromide. Our case was negative and not considered as a high-risk HPV status (Fig. 5).
Electrophoresis of human papillomavirus (HPV) status. The band in lane 3 represents negative reactivity for HPV in this case, whereas lanes 2 and 4 correspond to the controls, which were the HPV-positive cell line UMSCC-47 (a gift from Dr TE Carey) and H2O, respectively. The DNA size marker is located on lane 1.
In the head and neck, SmCC most commonly arises in the larynx, but has also been reported in the sinonasal tract and salivary glands (10,11). Combined SmCC of the larynx has only been reported in 17 cases in the literature to date. The majority of these patients were men and in the 6th-7th decade of life. Moreover, the majority of the patients succumbed to the disease within 2 years of diagnosis, even with adjuvant radiation and chemotherapy (12–14). Despite the rarity of these tumors, the clinical behavior of combined SmCC of the larynx appears to be similar to that of the hypopharynx. Metastasis from a primary lung SmCC must be carefully distinguished from a primary hypopharyngeal or laryngeal SmCC by imaging studies of the lung (15). In this case, FDG-PET revealed high-level accumulation in the hypopharynx, without evidence of a lung tumor or distant metastasis. A chest contrast CT scan confirmed the absence of a primary lung tumor.
According to the World Health Organization classification of head and neck tumors in 2005, neuroendocrine carcinomas may be classified as typical carcinoid, atypical carcinoid, and SmCC (16). Neuroendocrine types of SmCC associated with an SqCC component are referred to as combined carcinomas. They are unusual, representing <10% of all neuroendocrine types (17). Neuroendocrine neoplasms of the hypopharynx and larynx constitute a morphologicaly heterogeneous group of tumors, with considerable differences in clinical behavior and very different treatment strategies (12). Combined SmCC of the hypopharynx is extremely rare and is often difficult to pathologically diagnose prior to surgical treatment. Moreover, the prognosis is very poor due to early metastasis, without established treatment regimen (3). Of the 4 reported cases of combined SmCC of the hypopharynx, including our case, 3 succumbed to the disease within 1 year (Table I). Multi-modality therapy should be performed for combined SmCC of the head and neck region. Therefore, new therapeutic strategies are required to improve the survival rate. The present case reports new findings: Positive expression of KIT and PDGFRα in the SmCC element and positive expression of EGFR and PDGFRα in the SqCC element. Furthermore, to the best of our knowledge, the present study is the first to report a KIT and PDGFRα mutation analysis in combined hypopharyngeal SmCC. KIT and PDGFRα, both mapped to chromosome 4q12, have structural similarities with other PDGFR family members. A majority of gastrointestinal stromal tumors (GISTs) display a gain-of-function mutation in the KIT proto-oncogene that encodes the KIT protein. The majority of mutations occur in KIT exon 11, but mutations may also be found in exon 9 and rarely in exons 13 and 17. The PDGFRα gene is also very similar to the KIT gene, and PDGFRα mutations have been found in exons 12, 14 and 18. Terada et al (18) reported KIT protein expression in 100% and PDGFRα expression in 65% of small-cell lung carcinoma cases; however, there were no genetic mutations of KIT and PDGFRα in small-cell lung carcinoma (18). In a previously reported case of esophageal combined SmCC, KIT and PDGFRα were expressed in the SmCC component, but not in the SqCC component (5). It was found that SmCC of the lung and extrapulmonary organs expressed KIT and PDGFRα, but there were no mutations in these genes within the hot spots of GISTs. These findings are almost completely in accord with those of our case study.
No biomarker has been yet proven to predict response to targeted therapy in either SmCC or SqCC. Moreover, a predictive biomarker in one cancer type may not be helpful in another cancer type, suggesting that different mechanisms may be involved in combined SmCC. To the best of our knowledge, a molecular-targeted therapy for treating combined SmCC of the hypopharynx and larynx has not yet been reported. Our case is the first to report KIT and PDGFRα expression in combined SmCC in the hypopharynx and larynx; if similar results are obtained from larger series, these data may have management and prognostic implications through the possible use of targeted biological therapy in these tumors. At present, SmCC treatment remains a significant challenge for the oncologists, with several targeted agents under evaluation. However, there is no effective molecular-targeted therapy for SmCC. Evaluating the expression of the KIT and PDGFRα genes within hypopharyngeal SmCC may facilitate the development of novel agents for the molecular-targeted therapy of this tumor. However, further investigations are necessary regarding these proteins expression and clinical application of molecular targeted therapy for hypophageal combined SmCC.
The authors would like to thank Ms. Yuko Mohri for her excellent technical support.
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