J Pathol Transl Med.  2022 May;56(3):152-156. 10.4132/jptm.2021.12.09.

A sinonasal yolk sac tumor in an adult

Affiliations
  • 1Department of Pathology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea
  • 2Department of Otorhinolaryngology-Head and Neck Surgery, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea
  • 3Department of Pathology, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea

Abstract

Yolk sac tumors (YSTs), which are also called endodermal sinus tumors, are malignant tumors of germ cell origin. These tumors usually occur in the gonads, but 20% of cases have been reported at extragonadal sites. The head and neck is a rarely affected region that accounts for just 1% of all malignant tumors of germ cell origin. In addition, YSTs arise mostly in childhood. We present a rare pathologically pure case of primary adult YST in the sinonasal area. A 45-year-old male patient presented with a rapidly growing mass in the nasal cavity, which caused nasal obstruction and bloody post-nasal drip. The histopathologic features indicated pure YST, and immunohistochemical analysis revealed positive reactivity for Sal-like protein 4 and alpha-fetoprotein. Herein, we discuss the clinical, radiologic, and histologic features of this YST and review other cases of sinonasal YST in adults.

Keyword

Yolk sac tumor; Endodermal sinus tumor; Paranasal sinus; Nasal cavity; Adult

Figure

  • Fig. 1 Coronal (A) and transverse (B) magnetic resonance imaging shows a mass in the right nasal cavity and bilateral frontal sinus.

  • Fig. 2 Histopathologic findings of a sinonasal yolk sac tumor. (A) Reticular and microcystic growth patterns are observed with loose myxoid stroma. (B) A polyvesicular vitelline pattern is occasionally observed. (C) Schiller-Duval bodies are noted focally. (D) Intra- and extra-cytoplasmic hyaline globules are observed.

  • Fig. 3 On immunohistochemical staining, the tumor cells show diffuse strong nuclear positivity for Sal-like protein 4 (A) and diffuse strong cytoplasmic positivity for α-fetoprotein (B).

  • Fig. 4 Immunohistochemical staining revealed that the tumor cells were negative for p40 (A) and diffusely positive for integrase interactor 1 (B) and Brahma-related gene-1 (C).


Reference

References

1. Bernbeck B, Schneider DT, Bernbeck B, et al. Germ cell tumors of the head and neck: report from the MAKEI Study Group. Pediatr Blood Cancer. 2009; 52:223–6.
Article
2. Ronchi A, Cozzolino I, Montella M, et al. Extragonadal germ cell tumors: not just a matter of location: a review about clinical, molecular and pathological features. Cancer Med. 2019; 8:6832–40.
Article
3. Khan S, Jetley S, Pujani M, Neogi S. Pure yolk sac tumor of testis in an adult: a rare occurrence. J Postgrad Med. 2014; 60:351–3.
4. Nogales FF, Preda O, Nicolae A. Yolk sac tumours revisited: a review of their many faces and names. Histopathology. 2012; 60:1023–33.
Article
5. Agaimy A, Hartmann A, Antonescu CR, et al. SMARCB1 (INI-1)-deficient sinonasal carcinoma: a series of 39 cases expanding the morphologic and clinicopathologic spectrum of a recently described entity. Am J Surg Pathol. 2017; 41:458–71.
6. Manivel C, Wick MR, Dehner LP. Transitional (cylindric) cell carcinoma with endodermal sinus tumor-like features of the nasopharynx and paranasal sinuses: clinicopathologic and immunohistochemical study of two cases. Arch Pathol Lab Med. 1986; 110:198–202.
7. Filho BC, McHugh JB, Carrau RL, Kassam AB. Yolk sac tumor in the nasal cavity. Am J Otolaryngol. 2008; 29:250–4.
Article
8. Mishra A, El-Naggar AK, DeMonte F, Hanna EY. Endodermal sinus tumor of the paranasal sinuses. Head Neck. 2008; 30:539–43.
Article
9. Thomas J, Adegboyega P, Iloabachie K, Mooring JW, Lian T. Sinonasal teratocarcinosarcoma with yolk sac elements: a neoplasm of somatic or germ cell origin? Ann Diagn Pathol. 2011; 15:135–9.
Article
10. Mei X, Xia Y, Sasano H, Gao H. Sinonasal yolk sac (endodermal sinus) tumor in an adult female: a case report and review of the literature. APMIS. 2015; 123:810–4.
Article
11. Zamecnik M, Rychnovsky J, Syrovatka J. Sinonasal SMARCB1 (INI1) deficient carcinoma with yolk sac tumor differentiation: report of a case and comparison with INI1 expression in gonadal germ cell tumors. Int J Surg Pathol. 2018; 26:245–9.
Article
12. Wang P, Hou G, Li F, Cheng X. A case of primary sinonasal yolk sac tumor. Clin Nucl Med. 2020; 45:908–9.
Article
13. Oosterhuis JW, Looijenga LH. Human germ cell tumours from a developmental perspective. Nat Rev Cancer. 2019; 19:522–37.
Article
14. Hodgson A, Ghorab Z, Parra-Herran C. Somatically derived yolk sac tumor of the ovary in a young woman. Int J Gynecol Pathol. 2021; 40:296–300.
Article
15. Heerema-McKenney A, Harrison MR, Bratton B, Farrell J, Zaloudek C. Congenital teratoma: a clinicopathologic study of 22 fetal and neonatal tumors. Am J Surg Pathol. 2005; 29:29–38.
16. McKenney JK, Heerema-McKenney A, Rouse RV. Extragonadal germ cell tumors: a review with emphasis on pathologic features, clinical prognostic variables, and differential diagnostic considerations. Adv Anat Pathol. 2007; 14:69–92.
Article
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