Abstract
Rationale:
Myofibromas are rare benign spindle cell tumors of the soft tissue, bone, or internal organs that occur at any age. Here, we report a post-surgical thyroid bed myofibroma that mimicked a papillary thyroid carcinoma.
Patient concerns:
A 56-year-old male presented with a mass in the thyroid surgical bed, detected 3 years post thyroidectomy following papillary carcinoma.
Diagnosis:
Thyroid ultrasonography revealed a well-defined, lobulated, hypoechoic, solid nodule, with large rod-like echogenic foci in the thyroid surgical bed. The development of a postoperative suture granuloma was considered. However, ultrasonography performed 12 months later showed a marked increase in the lesion size. Two fine needle aspiration cytology yielded nondiagnostic results.
Intervention:
Considering the possibility of local tumor recurrence, surgical resection was performed.
Outcome:
The diagnosis of a myofibroma was confirmed, and no additional treatment was administered.
Lessons:
It is challenging to differentiate lesions occurring on the thyroid surgical bed after surgery, from recurrent thyroid cancer. A lesion measuring 6 mm, with a degree of punctate echogenicity, suggests tumor recurrence. Moreover, myofibromas are extremely rare. This case highlights that it is advisable to perform a core needle biopsy in cases of nondiagnostic fine needle aspiration results.
Keywords: core needle biopsy, fine needle aspiration, myofibroma, post-surgical thyroid bed, recurrence
1. Introduction
Myofibromas are rare benign spindle cell tumors composed of myofibroblasts that can occur in any age group. Infantile myofibromatosis, typically detected as solitary or multiple masses, commonly develop in those less than 2 years old.[1,2] In adults, myofibromas usually present as solitary superficial masses in any part of the body.[3] We report a post-surgical thyroid bed myofibroma that mimicked a recurrent papillary thyroid carcinoma. In our case, the tumor size increased significantly during the follow-up period and appeared to be in contact with the trachea, leading to the misdiagnosis of a local tumor recurrence of his thyroid cancer.
2. Case report
2.1. Patient information and clinical findings
A 56-year-old male presented with a mass in the thyroid surgical bed, detected via ultrasonography, 2 years post thyroidectomy for a papillary carcinoma. His thyroid function tests were normal, and he was asymptomatic. Ultrasonography revealed a well-defined, lobulated, hypoechoic, solid nodule, with large rod-like echogenic foci (Fig. 1A). The development of a postoperative suture granuloma was considered. However, ultrasonography performed 12 months later showed a marked increase in the lesion size (Fig. 1B and C). Because of the increased size of the lesion, the development of a recurrent papillary carcinoma was highly suspected.
Figure 1.
A 56-year-old male presented a thyroid surgical bed mass, detected via ultrasonography, 3 years after a total thyroidectomy for a papillary carcinoma. (A) Transverse ultrasound images revealed a 1.0 × 1.3 × 2.5 cm, irregularly-shaped, marked, hypoechoic lesion, with probable internal surgical clips. Ultrasound performed 12 months after the initial ultrasound. (B) Transverse ultrasound images showed a marked increase in the lesion size. (C) Doppler image showed no increased vascularity in the lesion.
Ultrasound-guided fine-needle aspiration (FNA) yielded nondiagnostic results. A repeat FNA was performed, as recommended by treatment guidelines,[4] however the results were still nondiagnostic.
2.2. Therapeutic interventions
Surgery was performed under the impression of a possible local tumor recurrence. Pre-operative workup, including contrast-enhanced neck computed tomography (CT) and positron emission tomography-CT (PET-CT), were performed. A heterogeneous hypermetabolic mass detected on PET-CT (Fig. 2A). Enhanced neck CT showed an ill-defined hypo-enhancing mass at right thyroid surgical bed (Fig. 2B), and a focal defect on the right side of the tracheal cartilage (Fig. 2C and D), suggested possible local tumor recurrence and invasion to the trachea.
Figure 2.
Preoperative imaging studies. (A) On 18F-fluorodeoxyglucose positron emission tomography-computed tomography, a right thyroid operative bed lesion showed heterogeneous hypermetabolism. (B) An axial computed tomography image showed an ill-defined hypo-enhancing mass at the right thyroid operative bed. (C) Axial and (D) coronal images showed focal decreased density at the right tracheal cartilage (arrow).
Excision of the neck mass was performed. A frozen biopsy of the resected specimen revealed a benign soft tissue. The patient was in a stable condition postoperative, and his thyroid function tests remained unremarkable.
2.3. Pathologic findings
The tumor was well-demarcated and consisted of spindle cells in a fibromyxoid background. The nuclei were elongated and tapered, and lacked nuclear atypia (Fig. 3A). Immunohistochemistry examination was performed to identify the nature of the spindle cells. The tumor cells stained focally for smooth muscle actin and did not express CD34, S100, or desmin (Fig. 3B). Based on the tumor microscopic and immunohistochemical features, this spindle cell tumor was consistent with a myofibroma.
Figure 3.
Histopathological examination of the surgical specimen. (A) Hematoxylin and eosin staining (×400), Specimen consisting of bland-looking spindle cells. (B) Immunohistochemical examination (SMA), the spindle cells expressed smooth muscle actin.
2.4. Ethical considerations
The institution review board approved the retrospective review of the medical records of this patient, and waived the requirement to obtain informed consent.
3. Discussion
Myofibromas are rare benign spindle cell tumors composed of myofibroblasts that can occur in any age group. This type of tumor is pathologically distinct from postoperative granulomas, which commonly occur in the surgical bed. Postoperative granulomas are characterized by myxoid substances and inflammatory cells.[5] Although some case reports have mentioned the occurrence of benign tumors after thyroidectomy, there are only a few reports on spindle cell tumors.[6,7]
Ultrasonography is the primary imaging modality for the detection of postoperative lesions and assessment of recurrent malignancies. Thyroid bed lesions are commonly seen on ultrasonography, and can occur in up to 40% of postoperative cases.[8] For effective management, it is essential to distinguish postoperative lesions from local tumor recurrences. Unfortunately, sonographic features, including cystic components, echogenicity, fatty hilum, and the tumor shape, are insufficient to differentiate local tumor recurrence. Only a lesion size of 6 mm or larger and the presence of punctate echogenic foci are considered significant indicators of local tumor recurrence.[8–12] Thus, when evaluating for possible tumor recurrence, it is crucial to consider not only the lesion sonographic features but also other clinical findings.
In particular, an increase in serum thyroglobulin (Tg) levels during serial follow-ups has been reported to significantly predict tumor recurrence.[13] However, some reports state the difficulty of predicting tumor recurrence based solely on serum Tg levels.[14] Thus, a comprehensive assessment that considers both sonographic features and serum Tg levels is necessary. In this case, the patient postoperative serum Tg level was < 0.2 ng/mL. Three years later, his Tg level increased to 2.15 ng/mL. Ultrasonography revealed a lesion measuring approximately 2.5 cm. Therefore, considering the criteria for sonographic features indicative of recurrence, particularly focusing on the lesion size and the accompanying slight elevation in serum Tg levels, local tumor recurrence was suspected.
FNA is a readily available and accurate method for evaluating head and neck masses. However, in the case of thyroid bed lesions, FNA may yield inconclusive results due to low cellularity or non-representative sampling.[15] Studies have reported a wide range (50%–95%) of conclusive results for FNAs of thyroidectomy bed lesions.[8,12,16,17] In our case, a repeat FNA was performed because of the initial non-diagnostic result, but it failed to provide a conclusive diagnosis. Recently, ultrasound-guided core needle biopsy (CNB) has been suggested as an adjunct to FNA, and has been reported to be accurate and safe for evaluating thyroidectomy bed lesions.[15] Considering the size of our patient lesion, which was larger than 2 cm, CNB could have been used as a complementary diagnostic tool.
4. Conclusion
Post-surgical thyroid bed myofibroma is challenging to differentiate from local tumor recurrence due to its rarity. Thus, in cases of thyroid bed nodules with nondiagnostic FNA results, it may be helpful to perform an additional CNB.
Author contributions
Supervision: Chi-Hoon Choi, Jisun Lee, Yook Kim, Yeongtae Park, Ok-Jun Lee.
Writing – original draft: Jun Hyeon Park.
Writing – review & editing: Kyung Sik Yi.
Abbreviations:
- CNB
- core needle biopsy
- CT
- computed tomography
- FNA
- fine needle aspiration
- Tg
- thyroglobulin
All data generated or analyzed during this study are included in this published article [and its supplementary information files].
The authors have no conflicts of interest to disclose.
This work was supported by the research grant of the Chungbuk National University Hospital in 2023.
How to cite this article: Park JH, Yi KS, Choi C-H, Kim Y, Lee J, Park Y, Lee O-J. Post-surgical thyroid bed myofibroma simulating a recurrent papillary thyroid carcinoma: A case report and review of the literature . Medicine 2024;103:2(e36945).
Contributor Information
Jun Hyeon Park, Email: eh19440@daum.net.
Chi-Hoon Choi, Email: chihoonc@naver.com.
Yook Kim, Email: sixtwin@hanmail.net.
Jisun Lee, Email: ojlee@chungbuk.ac.kr.
Yeongtae Park, Email: eh19440@daum.net.
Ok-Jun Lee, Email: ojlee@chungbuk.ac.kr.
References
- [1].Kempson RL, Fletcher CDM, Evans HL, Hendrickson MR, Siblet RK. Tumors of soft tissue. In: Atlas of Tumor Pathology. 1st ed. Amer Registry of Pathology; 2001:64–67. [Google Scholar]
- [2].Foss RD, Ellis GL. Myofibromas and myofibromatosis of the oral region: a clinicopathologic analysis of 79 cases. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2000;89:57–65. [DOI] [PubMed] [Google Scholar]
- [3].Beham A, Badve S, Suster S, et al. Solitary myofibroma in adults: clinicopathological analysis of a series. Histopathology. 1993;22:335–41. [DOI] [PubMed] [Google Scholar]
- [4].Cooper DS, Doherty GM, Haugen BR, et al. Revised American Thyroid Association management guidelines for patients with thyroid nodules and differentiated thyroid cancer. Thyroid. 2009;19:1167–214. [DOI] [PubMed] [Google Scholar]
- [5].Kang M, Ha SY, Cho HY, et al. Fine needle aspiration cytology of postoperative spindle cell nodule in neck after thyroidectomy: a case report. Korean J Pathol. 2013;47:89–91. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [6].Baloch ZW, Wu H, LiVolsi VA. Post-fine-needle aspiration spindle cell nodules of the thyroid (PSCNT). Am J Clin Pathol. 1999;111:70–4. [DOI] [PubMed] [Google Scholar]
- [7].Kim SW, Oh YL, Choi JY, et al. Postoperative spindle cell nodule after thyroidectomy: a case mimicking recurrence with anaplastic transformation of thyroid cancer. Head Neck. 2013;35:E13–7. [DOI] [PubMed] [Google Scholar]
- [8].Frates MC, Parziale MP, Alexander EK, et al. Role of sonographic characteristics of thyroid bed lesions identified following thyroidectomy in the diagnosis or exclusion of recurrent cancer. Radiology. 2021;299:374–80. [DOI] [PubMed] [Google Scholar]
- [9].Kamaya A, Gross M, Akatsu H, et al. Recurrence in the thyroidectomy bed: sonographic findings. AJR Am J Roentgenol. 2011;196:66–70. [DOI] [PubMed] [Google Scholar]
- [10].Lee JH, Lee HK, Lee DH, et al. Ultrasonographic findings of a newly detected nodule on the thyroid bed in postoperative patients for thyroid carcinoma: correlation with the results of ultrasonography-guided fine needle aspiration biopsy. Clin Imaging. 2007;31:109–13. [DOI] [PubMed] [Google Scholar]
- [11].Hahn SY, Shin JH, Han BK, et al. Predictive factors related to the recurrence at US-guided fine needle aspiration in postoperative patients with differentiated thyroid cancer. Clin Endocrinol (Oxf). 2011;74:270–5. [DOI] [PubMed] [Google Scholar]
- [12].Shin JH, Han BK, Ko EY, et al. Sonographic findings in the surgical bed after thyroidectomy: comparison of recurrent tumors and nonrecurrent lesions. J Ultrasound Med. 2007;26:1359–66. [DOI] [PubMed] [Google Scholar]
- [13].Xu S, Huang H, Zhang X, et al. Predictive value of serum thyroglobulin for structural recurrence following lobectomy for papillary thyroid carcinoma. Thyroid. 2021;31:1391–9. [DOI] [PubMed] [Google Scholar]
- [14].Park S, Jeon MJ, Oh HS, et al. Changes in serum thyroglobulin levels after lobectomy in patients with low-risk papillary thyroid cancer. Thyroid. 2018;28:997–1003. [DOI] [PubMed] [Google Scholar]
- [15].Jeong SY, Baek JH, Chung SR, et al. Diagnostic performance of core needle biopsy for characterizing thyroidectomy bed lesions. Korean J Radiol. 2022;23:1019–27. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [16].Bishop JA, Owens CL, Shum CH, et al. Thyroid bed fine needle aspiration: experience at a large tertiary care center. Am J Clin Pathol. 2010;134:335–9. [DOI] [PubMed] [Google Scholar]
- [17].Park DS, Cho JS, Park MH, et al. Malignant thyroid bed mass after total thyroidectomy. J Korean Surg Soc. 2013;85:97–103. [DOI] [PMC free article] [PubMed] [Google Scholar]



