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Inicio Cirugía Española (English Edition) Thymic cysts: A rare entity in adults
Información de la revista
Vol. 99. Núm. 1.
Páginas 71-73 (enero 2020)
Vol. 99. Núm. 1.
Páginas 71-73 (enero 2020)
Scientific letter
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Thymic cysts: A rare entity in adults
Quiste tímico: una entidad rara en el adulto
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Raquel Queralt Martín
Autor para correspondencia
raquelqueralt@gmail.com

Corresponding author.
, Miguel Ibáñez Belenguer, Andreu Martínez Hernández, Pedro Daniel Menor Durán, Jose Manuel Laguna Sastre
Servicio de Cirugía General y Digestiva, Hospital General Universitario de Castellón, Castellón, Spain
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The appearance of cervical tumors in adults is frequent, mainly due to the growth of thyroid nodules in the context of multinodular goiter. In some cases, these masses do not depend on the thyroid, so the differential diagnosis should include other types of rare lesions, including thymic cysts.

Thymic cysts account for 1% of cervical masses and appear mainly in the first decade of life,1 so they are very rare in adults.2,3 They tend to present as an asymptomatic cervical mass, and in many cases the diagnosis is made after the lesion is resected, since preoperative imaging tests do not determine the etiology of the cyst.4 Recurrence after complete excision has not been documented in the literature.5

We present the case of a 36-year-old woman with no relevant history who consulted for an asymptomatic left anterior cervical mass that had been developing over several months. Ultrasound detected a 4-cm nodule with a cystic appearance that did not depend on the thyroid. CT scan located the lesion below the thyroid gland, posterior to the infrahyoid muscles and anterior to the trachea, in contact with the right brachiocephalic trunk as well as the origin of the right common carotid artery, but no signs of invasion (Fig. 1). The study was completed with an MRI that demonstrated a cystic image measuring 4 cm with no extension to the thorax, which did not depend on any structure and presented benign characteristics.

Fig. 1.

Computed tomography scan: A) sagittal view showing a cystic lesion below the thyroid gland; B) axial view showing that the cystic lesion does not invade the neighboring structures.

(0.1MB).

The patient was treated surgically, making a transverse cervical incision and observing an anterior cervical cystic-looking lesion that extended to the superior mediastinum, without invading any structure (Fig. 2). It was removed without incident, preserving the recurrent laryngeal nerves and the inferior parathyroid glands, and the patient was discharged 24 h after the intervention.

Fig. 2.

Intraoperative image of the cystic lesion (arrow) in the anterior cervical region, not adhered to adjacent structures.

(0.07MB).

The histopathological study reported a unilocular thymic cyst with cuboidal epithelium, thymic tissue, and an adjacent ectopic parathyroid gland.

During embryonic development, the thymus arises from the 3rd pair of pharyngeal pouches next to the inferior parathyroid glands. During the 7th week of gestation, the primordium of the thymus migrates from the angle of the mandible to the superior mediastinum, forming the thymopharyngeal duct, which later becomes fibrous.6

Thymic cysts are very rare and appear mainly in children, although cases have been described in adults, especially during the 2nd and 3rd decades,2,5 affecting men more often. They are more frequently located on the left side, although they can appear at any point from the upper edge of the hyoid bone to the antero-superior mediastinum, and their size varies (1-17 cm). Most are asymptomatic, although they can cause dyspnea, dysphagia and voice alterations.1,5

Although various classifications have been described, the most widely accepted today divides them into congenital and acquired forms. The former are due to a persistence of the thymopharyngeal duct, while the latter are due to degeneration of the ectopic thymic tissue.3,5,7,8

In most cases, the diagnosis is made after analysis of the surgical specimen,4 as in the case described. Preoperative imaging tests, such as ultrasound, CT and MRI, are useful to characterize the lesion and determine its relationship with neighboring structures, although they hardly provide an etiological diagnosis. Needle aspiration is not useful to determine the origin of cervical cystic lesions in most cases.4

The differential diagnosis should be made with other cervical cystic lesions, such as thyroglossal duct cyst, branchial cyst, thyroid cyst, desmoid cyst, lymphangiomas, cystic teratoma, lymphadenopathy with a cystic appearance, metastases, and other causes that are very rare but should be considered in adults, such as parathyroid cysts.5,9 In the latter case, biochemical analysis of the cyst fluid is useful, since it will present a high level of PTH.9 The possibility of malignant degeneration must also be considered, since the presence of a thymic carcinoma within a thymic cyst has been described in the literature.10

Thymic cysts can be uni- or multilocular and have an epithelium that can be squamous, cuboidal, or columnar. The histopathological characteristics that determine the diagnosis and are considered pathognomonic are the presence of thymic tissue remnants in the wall and the presence of Hassall’s corpuscles, which are eosinophilic structures present in the normal thymic medulla.1,8 Furthermore, as a consequence of the common embryological origin, it is common to find parathyroid tissue adjacent to the cyst wall, as described in the clinical case we have presented.

Treatment is surgical, with complete excision of the lesion. No recurrences have been described in the literature, so the prognosis is excellent.5

In conclusion, thymic cysts are rare in adults but should be included in the differential diagnosis of cervical lesions.

References
[1]
M. Betti, N.H. Hoseini, A. Martin, A. Buccoliero, A. Messineo, M. Ghionzoli.
Cervical Thymic Cyst in Childhood: A Case Report.
Fetal Pediatr Pathol, 34 (2015), pp. 65-69
[2]
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[3]
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[8]
M. Haro-García, J. Crespo Del Hierro, R. de la Fuente-Cañibano, M.A. Alañón-Fernández.
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[9]
J.A. Amondarain Arratíbel, X. Aribe, C. Olalla, M. Echenique Elizondo.
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[10]
S.I. Yamashita, H. Yamazaki, T. Kato, T.A. Yokota, N. Matsumoto, S. Matsukura.
Thymic Carcinoma which Developed in a Thymic Cyst.
Intern Med, 35 (1996), pp. 215-218

Please cite this article as: Queralt Martín R, Ibáñez Belenguer M, Martínez Hernández A, Menor Durán PD, Laguna Sastre JM. Quiste tímico: una entidad rara en el adulto. Cir Esp. 2021;99:71–73.

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