- Case report
- Open Access
- Open Peer Review
Spindle cell sarcomatoid carcinoma of the trachea: first case report of surgical resection
© The Author(s). 2016
- Received: 21 May 2016
- Accepted: 28 July 2016
- Published: 5 August 2016
Primary malignant tracheal tumors are rare, accounting for approximately 0.2 % of respiratory tract tumors yearly, with squamous cell carcinomas and adenoid cystic carcinomas accounting for two-thirds of these cases. Sarcomatoid carcinomas are a group of poorly differentiated non-small cell lung carcinomas containing a component of sarcoma or sarcoma-like (spindle and/or giant cell) differentiation, categorized into five morphologic subgroups. Spindle cell sarcomatoid carcinoma is a rare variant of sarcomatoid carcinomas, consisting of only spindle-shaped tumor cells. Only one other case has been reported as a primary tracheal tumor.
We present a 75-year-old male, having progressive dyspnea and cough, with a spindle cell sarcomatoid carcinoma tumor visualized on chest computed tomography scan and confirmed with biopsy.
Due to its low incidence, knowledge of treatment methods, prognostic factors, and etiology is limited thus approaches to eradication have widely varied. We are reporting the second published case of spindle cell sarcomatoid carcinoma of the trachea and the first reported successful outcome of definitive treatment with tracheal resection.
- Spindle cell
Primary tracheal tumors are rare, with malignancy occurring at a rate of 0.1 new cases per 100,000 every year, corresponding to 0.2 % of all tumors involving the respiratory tract . Primary tracheal cancers are more common in current or former male cigarette smokers, with peak incidence in the sixth decade of life [2, 3]. Due to the central location and tendency to protrude into the lumen of the large airways, patients typically present with symptoms of dry cough, hemoptysis, progressive dyspnea, hoarseness, and fevers secondary to recurrent pneumonia, often leading to misdiagnosis of asthma or chronic pulmonary disease [4, 5]. Squamous cell carcinoma (SCC) and adenoid cystic carcinoma (ACC) make up nearly two thirds of primary tracheal cases. Tracheal tumors apart from these are extremely uncommon and consist of a heterogeneous group of benign and malignant tumors, with only one other reported case of primary tracheal spindle cell carcinomas to date [6, 7].
Spindle cell carcinoma belongs to a group of poorly differentiated non-small cell carcinomas known as sarcomatoid carcinomas. According to the World Health Organization 2004 classifications of lung tumors, this group contains components of sarcoma or sarcoma-like (spindle cell or giant cell) differentiation, consisting of only spindle shaped cells that form cohesive nests and irregular fascicles of malignant cells with features including nuclear hyperchromasia and distinct nucleoli . These tumor masses include scattered and focally dense regions of lymphoplasmacytic infiltrates throughout .
Due to the rarity of these tracheal cases, there is often a delay in diagnosis and inappropriate treatment approaches . Additionally, no universally accepted TNM classification for tracheal malignancies exists, and proposed staging systems are based on a small number of considered cases [1, 8]. Generally, tracheal carcinomas have poor prognosis, with 5-year survival rates of up to 15 % and 10-year survival rates of 7 % . On the other hand, the spindle cell group of carcinomas are described to be aggressive and thought to have worse clinical outcomes than conventional non-small cell carcinomas. Five-year survival rates are only 20 % despite many patients presenting with stage I disease . Adjuvant chemotherapy and radiation do not seem to play a helpful role in treatment of spindle cell type tumors, and thus resection remains the mainstay of tumor eradication . Here we report a case of a former smoker presenting with progressive dyspnea, discovered to have primary tracheal spindle cell sarcomatoid carcinoma treated definitively with surgical resection.
A 75 year-old Caucasian male presented with progressively worsening dyspnea of eight days, wheezing and productive cough with clear sputum. His symptoms began abruptly, worsened upon exertion, and were unrelieved by home albuterol inhaler. The patient is a former smoker with a 52 pack-year history, quitting four years prior to the onset of his symptoms. His past medical history is significant for chronic obstructive pulmonary disease (COPD) and atherosclerotic disease involving his peripheral and carotid arteries. His past surgical history is unremarkable, and lungs were clear to auscultation with stridor on physical exam at the time of his presentation.
Following the procedure, the patient reported improvement in breathing and stridor. After an eight-day hospital course, he self-ambulated on room air, tolerated oral intake, and denied pain or difficulty swallowing or breathing. At his six month post-operative follow-up, he continued to do well without complications or evidence of recurrence. The patient is under observation by both surgery and oncology, with regularly scheduled CT scans to monitor for recurrence.
Surgical management is well established as the definitive treatment for primary tracheal tumors [9, 10, 14]. Resectability of these tumors depends most on locoregional disease characteristics over distant characteristics and is associated with survival superior to palliative therapy, especially when complete resection with negative margins is achieved . The role for adjuvant therapy with chemotherapy or radiation is variable and most recommendations are based on retrospective analysis for non-specific squamous cell histology-associated outcomes  and/or for cases where there is advanced disease, other than R0 resection, unresectable tumors or when the patient is not a surgical candidate. Among patients with tracheal tumors, survival in those undergoing complete resections is significantly longer than those undergoing alternative modalities of treatment, although the rarity of these tumors and complexity in selecting treatment options has allowed for limited analysis of outcomes [5, 16].
In the first reported case of primary tracheal spindle cell carcinoma, cisplatin-based chemotherapy with radiation was the treatment chosen by patient preference, however, the regimen was not completed due to patient death within five months of diagnosis . In our case, a complete tracheal sleeve resection was performed, with anastomosis of the regions above and below the resected region (Figs. 2 and 3). Resection alone has thus far proved to be effective in management of this rare case, as the patient has been without complications throughout his postoperative period. Further follow up will be needed to assess the long-term success of this treatment option.
Spindle cell carcinoma or sarcomatoid carcinoma of the trachea is an uncommon tumor. Because the lesion caused greater than a fifty-percent reduction in trachea luminal diameter, this patient experienced obstructive symptoms such as dyspnea and cough resulting in early detection prior to metastasis. The isolated nature of disease allowed for successful tracheal resection.
As various tracheal tumors have been characterized across reviews, corresponding treatment approaches have widely varied with little evidence pointing towards a single best modality for management . The operative technique described here may serve as a principal reference for future tracheal spindle cell sarcomatoid carcinomas with similar properties. Additionally as more cases are reported, this case contributes to a better understanding of tumor growth predilection along the trachea, tumor size, and possible distant metastasis, allowing for improved assessment of appropriate surgical candidates and higher long-term survival with reduced operative morbidity and mortality.
ACC, Adenoid cystic carcinoma; COPD, Chronic obstructive pulmonary disease; CT, Computed tomography; SCC, Squamous cell carcinoma
We would like to thank Dr. Sean Fitzgerald for providing the pathological data and images used here, and for his time in discussing the relevant pathological features and significance of the tumor mentioned.
We would like to acknowledge the Research Open Access Publishing (ROAAP) Fund of the University of Illinois at Chicago, for financial support towards the open access publishing fee for this article.
Availability of data and materials
RA, JG, DD, and EA performed the surgical intervention described, including diagnostic work up and follow up care of the patient. NH and EY collected data, reviewed literature, and wrote the initial transcript. All authors read, edited, and approved the final manuscript.
RA is Section Chief of Cardiothoracic Surgery in the Department of Surgery at University of Illinois College of Medicine in Peoria.
The authors declare that they have no competing interests.
Consent for publication
Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of the Journal of Cardiothoracic Surgery.
Ethics approval and consent to participate
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
- Junker K. Pathology of tracheal tumors. Thorac Surg Clin. 2014;24(1):7–11.View ArticlePubMedGoogle Scholar
- Honings J, van Dijck JA, Verhagen AF, van der Heijden HF, Marres HA. Incidence and treatment of tracheal cancer: a nationwide study in the Netherlands. Ann Surg Oncol. 2007;14(2):968–76.View ArticlePubMedGoogle Scholar
- Allen MS. Malignant tracheal tumors. Mayo Clin Proc. 1993;68(7):680–4.View ArticlePubMedGoogle Scholar
- Corrin B, Chang YL, Rossi G, Koss MN, Geisinger K, Wick MR, Nappi O, Finkelstein SD, Nakatani Y. Sarcomatoid carcinoma. In: Travis WD, Brambilla E, Müller-Hermelink HK, Harris CC, editors. Pathology and genetics of tumours of the lung, pleura, thymus and heart. Lyon, France: IARC Press; 2004. p. 53–8.Google Scholar
- Webb BD, Walsh GL, Roberts DB, Sturgis EM. Primary tracheal malignant neoplasms: the University of Texas MD Anderson cancer center experience. J Am Coll Surg. 2006;202(2):237–46.View ArticlePubMedGoogle Scholar
- Gaissert HA, Grillo HC, Shadmehr MB, Wright CD, Gokhale M, Wain JC, Mathisen DJ. Uncommon primary tracheal tumors. Ann Thorac Surg. 2006;82(1):268–73.View ArticlePubMedGoogle Scholar
- Aksu K, Aktas Z, Aksu F, Orsel O, Demirag F, Sipit T, Firat GS. Spindle cell sarcomatoid carcinoma: first case reported in the trachea. Tuberk Toraks. 2009;57(3):337–41.PubMedGoogle Scholar
- Macchiarini P. Primary tracheal tumours. Lancet Oncol. 2006;7(1):83–91.View ArticlePubMedGoogle Scholar
- Grillo HC, Mathisen DJ. Primary tracheal tumors: treatment and results. Ann Thorac Surg. 1990;49(1):69–77.View ArticlePubMedGoogle Scholar
- Honings J, Gaissert HA, van der Heijden HF, Verhagen AF, Kaanders JH, Marres HA. Clinical aspects and treatment of primary tracheal malignancies. Acta Otolaryngol. 2010;130(7):763–72.View ArticlePubMedGoogle Scholar
- Gaissert HA, Grillo HC, Shadmehr MB, Wright CD, Gokhale M, Wain JC, Mathisen DJ. Long-term survival after resection of primary adenoid cystic and squamous cell carcinoma of the trachea and carina. Ann Thorac Surg. 2004;78(6):1889–97.View ArticlePubMedGoogle Scholar
- Li Y, Peng A, Yang X, Xiao Z, Wu W, Wang Q. Clinical manifestation and management of primary malignant tumors of the cervical trachea. Eur Arch Otorhinolaryngol. 2014;271(2):225–35.View ArticlePubMedGoogle Scholar
- Merritt RE, Mathisen DJ. Tracheal Resection. In: Patterson GA, Cooper JD, Deslauriers J, Lerut A, Luketich JD, Rice TW, Pearson FG, editors. Pearson’s Thoracic and Esophageal Surgery. 3rd ed. Philadelphia: Elsevier Churchill Livingstone; 2008. p. 376–82.View ArticleGoogle Scholar
- Grillo HC. Tracheal tumors: surgical management. Ann Thorac Surg. 1978;26(2):112–25.View ArticlePubMedGoogle Scholar
- Xie L, Fan M, Sheets NC, et al. The use of radiation therapy appears to improve outcome in patients with malignant primary tracheal tumors: A SEER-based analysis. Int J Radiat Oncol. 2012;84:464–70.View ArticleGoogle Scholar
- Regnard JF, Fourquier P, Levasseur P. Results and prognostic factors in resections of primary tracheal tumors: A multicenter retrospective study. J Thorac Cardiovasc Surg. 1996;111(4):808–14.View ArticlePubMedGoogle Scholar