Printer Friendly
The Free Library
22,741,889 articles and books

Yolk sac tumor of the temporal bone: Report of a case.



Abstract

Yolk sac tumor (endodermal sinus tumor endodermal sinus tumor
n.
A malignant neoplasm occurring in the gonads, in sacrococcygeal teratomas, and in the mediastinum and producing alpha-fetoprotein. Also called yolk-sac tumor.
) is rarely encountered in the temporal bone. Facial nerve paralysis can be a primary manifestation of this condition. Histologically, the tumor can be difficult to diagnose, although elevated levels of alpha fetoprotein can facilitate its identification.

In this report, we describe the case of an 18-month-old girl who developed peripheral VIIth nerve palsy and a polypoid mass in the left external ear canal 3 months following myringotomy myringotomy /my·rin·got·o·my/ (mi-ring-got´ah-me) tympanotomy; creation of a hole in the tympanic membrane, as for tympanocentesis.

myr·in·got·o·my
n.
. Computed tomography and magnetic resonance imaging magnetic resonance imaging (MRI), noninvasive diagnostic technique that uses nuclear magnetic resonance to produce cross-sectional images of organs and other internal body structures.  revealed that the tumor involved the left external ear canal, middle ear space, and mastoid air cells. Biopsies were consistent with a yolk sac tumor. Special staining demonstrated that only a very few tumor cells were positive for alpha fetoprotein, despite the markedly elevated level of alpha fetoprotein in her serum. The patient was treated with chemotherapy, which included cisplatin, etoposide, and bleomycin. Within a period of weeks, she experienced a complete reversal of her left VIIth nerve palsy, a marked decrease in her serum alpha fetoprotein levels, and a dramatic resolution of the tumor as demonstrated radiographically. Such a successful chemotherapeutic response in this case argues against surgical intervention in other cases, particularly in view of the risk of serious complications with surgery.

Introduction

Yolk sac tumor (endodermal sinus tumor) of the head and neck region is extremely rare. [1] In the English-language literature, only two cases of yolk sac tumor of the temporal bone have been described. [23] In this report, we present a rare case of an 18-month girl with a rapidly progressive and extensive yolk sac tumor. This patient presented with bilateral otitis media with effusions, which necessitated bilateral myringotomies and placement of pressure-equalizing tubes. Three months later, she returned with an enlarged left aural polyp and ipsilateral facial nerve palsy facial nerve palsy Facial palsy, see there . The rapid growth of the tumor required multiple biopsies for histopathologic confirmation. Markedly elevated serum alpha fetoprotein levels facilitated the diagnosis. A dramatic response to chemotherapy, which included a complete resolution of the facial nerve paralysis, was subsequently observed. In this article, we report the morphologic features of the tumor and review the investigative procedures.

Case report

The patient was born to a 26-year-old mother in October 1994. There were no complications during the pregnancy and delivery. During her first year of life, the patient developed recurrent bilateral otitis media. In December 1995, she underwent bilateral myringotomies and placement of pressure-equalizing tubes. Serous serous /se·rous/ (ser´us)
1. pertaining to or resembling serum.

2. producing or containing serum.


se·rous
adj.
Containing, secreting, or resembling serum.
 effusions, but no other abnormalities, were noted at this time.

In March 1996, the patient was taken to the emergency room with left peripheral VIIth nerve palsy and left otorrhea. The paresis failed to improve after treatment with antibiotics and steroids. Physical examination revealed a large polyp in the left external auditory canal external auditory canal
n.
See ear canal.
 (figure 1A), cloudy left otorrhea, and a left peripheral VIIth nerve palsy (figure 1B). Biopsies from the mass were suspicious but inconclusive for malignancy.

Computed tomography (CT) without contrast of the temporal bone revealed that a soft tissue mass filled the left external auditory canal, middle ear space, and mastoid air cells. Although the ossicular os·si·cle  
n.
A small bone, especially one of the three bones of the middle ear.



[Latin ossiculum, diminutive of os, bone; see ost- in Indo-European roots.
 chain was intact, there was some dehiscence dehiscence /de·his·cence/ (de-his´ins) a splitting open.

wound dehiscence  separation of the layers of a surgical wound.


de·his·cence
n.
 of the external auditory canal, which suggested a confluence of the mass with the parotid gland. Magnetic resonance imaging (MRI) of the head revealed the presence of a large mass that involved the entire left temporal bone and extended to the left cerebellopontine angle cistern (figure 2). No abnormal vasculature was noted.

The patient failed to improve on antibiotics. Laboratory studies revealed that her serum alpha fetoprotein level was 7,020 ng/ml (normal: 0-10). Her serum chemistry panel, liver function test, coagulation coagulation (kōăg'ylā`shən), the collecting into a mass of minute particles of a solid dispersed throughout a liquid (a sol), usually followed by the precipitation or  profile, urinalysis, and beta human chorionic gonadotropin human chorionic gonadotropin (HCG): see gonadotropic hormone.  and carcinoembryonic antigen levels were well within normal limits. CT studies of the chest, abdomen, and pelvis were normal, and a technetium bone scan showed increased uptake only in the area of the left temporal bone. Bone marrow aspirate and cerebrospinal fluid studies also were negative. The patient was taken to the operating room in April 1996 for further biopsies and debulking of the lesion, which by that time had grown to fill the entire left external auditory canal.

The biopsy specimen consisted of several fragments of tan to red tissue and measured 1.1 x 0.5 x 0.4 cm in aggregate. Sections from the tumor were fixed in 10% buffered formalin and in B-5 fixative. The tissue was processed routinely, and paraffin-embedded sections were stained with hematoxylin and eosin for immunohistochemical studies. A Ventana automatic stainer was used for the immunohistochemical studies. The antibodies used and the results of the staining are listed in the table. Tissue for ultrastructural examination was fixed in glutaraldehyde. The tissue was osmicated, dehydrated in ethanol, and embedded in epoxy resin in the conventional manner. Sections were examined with a Phillips-Zeiss transmission electron microscope.

Microscopic examination showed that a mixed glandular and sheet-like arrangement of tumor had infiltrated the dermis and soft tissue of the external ear canal. The tumor cells contained vacuolated vacuolated /vac·u·o·lat·ed/ (vak´u-o-lat?ed) containing vacuoles.

vac·u·o·lat·ed or vac·u·o·late
adj.
Containing vacuoles or a vacuole.



vacuolated

containing vacuoles.
 cytoplasm and a single large vesicular nucleus. Small eosinophilic eosinophilic /eo·sin·o·phil·ic/ (-fil´ik)
1. readily stainable with eosin.

2. pertaining to eosinophils.

3. pertaining to or characterized by eosinophilia.
 hyaline hyaline /hy·a·line/ (hi´ah-lin) glassy and translucent.

hy·a·line
adj.
Resembling glass, as in translucence or transparency; glassy.

n.
1.
 globules were noted in the cytoplasm. In one area, the tumor cells were arranged around a central blood vessel, which was surrounded by a space lined with tumor cells, which formed a Schiller-Duval body (figure 3). Periodic acid-Schiff (PAS)-stained sections showed numerous PAS-positive hyaline cytoplasmic bodies. Mitotic figures were numerous. The tumor cells showed a strong positivity for cytokeratin and vimentin. Desmin, S-100 protein, chromogranin, synaptophysin, somatostatin, and factor VIII showed negative staining within tumor cells. Only a very few tumor cells showed strong alpha fetoprotein positivity.

On electron microscopy, the tumor cells contained abundant cytoplasm, irregular nuclei, and a single prominent nucleolus nucleolus: see cell. . The cells showed apical microvilli microvilli
(mī´krōvil´ē),
n.pl tiny hairlike processes that extend from the surface of many cells. They are usually so small as to be visible only with an electron microscope.
 and were connected by well-developed junctional complexes. The tumor cell cytoplasm contained scattered mitochondria, profiles of rough endoplasmic reticulum rough endoplasmic reticulum

parts of the endoplasmic reticulum to which ribosomes are attached on the cytoplasmic side; involved in the biosynthesis of proteins for export to the outside of the cell and enzymes to be incorporated into cellular organelles such as lysosomes.
, Golgi's apparatus, and a few nonspecific intermediate filaments and particulate glycogen (figure 4).

The patient was started on chemotherapy with cisplatin, etoposide, and bleomycin. The tumor responded dramatically (figure 5). Clinically, the patient experienced a complete resolution of her facial nerve palsy (figure 6), and her serum alpha fetoprotein levels returned to normal (4.6 ng/ml). Followup CT and MRI CT and MRI
Two high technology methods of creating images of internal organs. Computerized axial tomography (CT or CAT) uses x rays, while magnetic resonance imaging (MRI) uses magnet fields and radio-frequency signals. Both construct images using a computer.
 studies revealed a dramatic regression of the tumor (figure 7). In total, the patient received ten cycles of chemotherapy.

At the time this paper was finalized, the patient had been followed for more than 36 months since her last treatment. Her serum alpha fetoprotein level was 2.4 ng/ml, and she was doing well.

Discussion

Yolk sac tumor is the most common malignant germ tumor found in infants. The sacrococcygeal sacrococcygeal /sa·cro·coc·cy·ge·al/ (sa?kro-kok-sij´e-al) pertaining to the sacrum and coccyx.

sac·ro·coc·cyg·e·al
adj.
Of, relating to, or affecting the sacrum and coccyx.
 area is the most common site of involvement in both newborns and infants. [4] In older children, the primary locations are the ovaries and the testes. [5,6] Less common primary sites include the pineal glands, third ventricle, anterior mediastinum, vagina, vulva, retroperitoneum, diaphragm, liver, and orbit. [2,7-9]

Primary yolk sac tumor rarely occurs in the temporal bone. [1-3] In the case presented here, a large and locally invasive mass was discovered occupying the left temporal bone, eroding the mastoid cortex, extending into the parotid gland, and involving the skull base. The diagnosis of yolk sac tumor was reached after a careful evaluation of the clinical presentation as well as the microscopic findings. The determinant points were the elevated serum alpha fetoprotein level, the histology of the tumor, and the dramatic response to triple-drug chemotherapy. Although mildly elevated serum alpha fetoprotein levels can be encountered in nonneoplastic conditions such as cirrhosis, hepatitis, and pregnancy, neoplasms that arise in the liver and germ cells (as well as the pancreas and stomach on rare occasions) can result in tremendously high elevations. Following adequate resection of these tumors, the serum alpha fetoprotein level drops rapidly, thus making it a sensitive marker of response to therapy. As seen in thi s case, histologic staining for alpha fetoprotein in these tumor cells is not 100% sensitive; in fact, alpha fetoprotein negativity in yolk sac tumors has been reported in 7% of tumors in the pediatric age groups. [10]

The differential diagnoses of a mass lesion of the temporal bone in pediatric age groups include rhabdomyosarcoma rhabdomyosarcoma /rhab·do·myo·sar·co·ma/ (mi?o-sahr-ko´mah) a highly malignant tumor of striated muscle derived from primitive mesenchymal cells. , congenital cholesteatoma, lymphoma, hemangioma hemangioma

Congenital benign tumour made of blood vessels in the skin. Capillary hemangioma (nevus flammeus, port-wine stain), an abnormal mass of capillaries on the head, neck, or face, is pink to dark bluish-red and even with the skin. Size and shape vary.
, teratoma teratoma /ter·a·to·ma/ (ter?ah-to´mah) pl. terato´mata, teratomas   a true neoplasm made up of different types of tissue, none of which is native to the area in which it occurs; usually found in the ovary or testis. , meningocele meningocele /me·nin·go·cele/ (me-ning´gah-sel) hernial protrusion of the meninges through a defect in the cranium (cranial m.) or vertebral column (spinal m.) .

me·nin·go·cele
n.
, dermoid cyst, undifferentiated carcinoma, and endolymphatic sac tumors. The endolymphatic sac, located between the dura and the posterior surface of the petrous portion of the temporal bone The petrous portion of the temporal bone or pyramid is pyramidal and is wedged in at the base of the skull between the sphenoid and occipital. Directed medialward, forward, and a little upward, it presents for examination a base, an apex, three surfaces, and three angles, , originates in the neuroectoderm and is lined with both columnar and simple cuboidal epithelium. Tumors that arise from the endolymphatic sac tend to be low-grade adenocarcinomas; a few cases are associated with von Hippel-Lindau disease von Hip·pel-Lindau disease or von Hippel-Lindau syndrome
n.
See Lindau's disease.


von Hippel-Lindau disease 
." [11-13] A papillary papillary /pap·il·lary/ (pap´i-lar?e) pertaining to or resembling a papilla, or nipple.
papillary,
adj similar to a small, nipple-shaped elevation or projection.
 variant of this tumor occurs predominantly in women, and takes on a more aggressive clinical course. [14-15] These tumors are positive by S-100 protein and negative for alpha fetoprotein. None of these tumors has been associated with elevated serum alpha fetoprotein levels. Glomus tumors (paragangliomas), the most common neoplasms arising from the middle ear, should also be considered in the differential diagnosis. [16-18] Microscopically, the tumor is highly vascular and divided by nests or "cell balls" composed of large ovoid-shaped cells with amphophilic cytoplasm. Immunohistochemically, the paraganglioma cells are reactive for catecholamines Catecholamines
Family of neurotransmitters containing dopamine, norepinephrine and epinephrine, produced and secreted by cells of the adrenal medulla in the brain.
, neuron-specific enolase, chromogranin, and synaptophysin. Ultrastructurally, the cells contain numerous dense-core granules of the neurosecretory neurosecretory

pertaining to or emanating from the secretory activities of nerve cells.


neurosecretory bodies
the form in which neurosecretions are passed along axons to release them into the blood.
 type.

Histologically, the yolk sac tumor can be difficult to diagnose, as exemplified by the need to repeatedly perform biopsies in our patient. This tumor has different histologic patterns: typical (reticular reticular /re·tic·u·lar/ (-lar) resembling a net.

re·tic·u·lar or re·tic·u·lat·ed
adj.
Resembling a net in form; netlike.
, solid, papillary, parietal), polyvesicular, hepatoid, glandular, and mixed. [6] In our patient, the tumor cells were arranged in a mixed pattern of solid-sheet and glandular formation with indistinct lumina. The tumor cells had a single vesicular nucleus and vacuolated cytoplasm. PAS-positive hyaline globules were identified in the cytoplasm of several cells. Schiller-Duval bodies were present. The tumor cells were strongly positive for cytokeratin and vimentin. S-100 protein, chromogranin, synaptophysin, and desmin were all negative. Although only a very few tumor cells were positive for alpha fetoprotein, the serum alpha fetoprotein level was markedly elevated.

To our knowledge, this is only the third reported case of a yolk sac tumor that involved the temporal bone. Given the rarity of this tumor in this location, no definitive treatment has been established. [2,3] A combination of surgical excision and chemotherapy has been the mainstay of treatment for ovarian yolk sac tumors. [5] However, in the temporal bone, where critical structures such as the facial nerve and internal carotid artery are involved, surgical excision might not be a feasible option. The role of radiation therapy has not been clearly established. Radiation might have an adjunctive role when it is selectively applied, but it must be administered with extreme caution in the pediatric age group. In our patient, the dramatic and favorable response to triple-drug chemotherapy has deferred the need for additional treatment. A similar response to chemotherapy was noted in the two previously reported cases of yolk sac tumor of the temporal bone. [23]

From the Department of Surgery, Division of Otolaryngology (Dr. Frank and Dr. Anand), and the Department of Pathology (Dr. Subramony), University of Mississippi Medical Center University of Mississippi Medical Center (UMC) is the health sciences campus of the University of Mississippi (Ole Miss). Located in Jackson, Mississippi (USA), it houses the Schools of Medicine, Dentistry, Nursing, Health Related Professions, and Graduate Studies in the Health , Jackson.

References

(1.) Devaney KO, Ferlito A. Yolk sac tumors (endodermal sinus tumors) of the extracranial extracranial

external to the cranial vault.


extracranial convulsions
when the cause of the convulsions is external to the brain, e.g. hypocalcemic tetanic convulsions.
 head and neck regions. Ann Otol Rhinol Laryngol 1997;106:254-60.

(2.) Kebudi R, Ayan I, Darendeliler E, et al. Non-midline endodermal sinus tumor in the head and neck region: A case report. Med Pediatr Oncol 1993;21:685-9.

(3.) Stanley RJ, Scheithaner BW, Thompson El, et al. Endodermal sinus tumor (yolk sac tumor) of the ear. Arch Otolaryngol Head Neck Surg 1987;113:200-3.

(4.) Keslar PJ, Buck JL, Suarez ES. Germ cell tumors of the sacrococcygeal region: Radiologic-pathologic correlation. Radiographics 1994;14:607-20.

(5.) Scully RE. Endodermal sinus tumor. In: Rosai j; ed. Tumors of the Ovary and Maldeveloped Gonads. Washington, D.C.: Armed Forces Institute of Pathology Armed Forces Institute of Pathology A section of the US military which provides consultations, reference atlases and educational programs for pathologists , Second Series #16, 1981.

(6.) Mostofi FK, Price EB. Tumors of the testes in children. In: Rosai J, ed. Tumors of the Male Genital System. Washington, D.C.: Armed Forces Institute of Pathology, Second Series #18, 1973.

(7.) Kirikae M, Arai H, Hidaka T, et al. Pineal pineal /pin·e·al/ (pin´e-il)
1. pertaining to the pineal body.

2. shaped like a pine cone.


pin·e·al
adj.
1. Having the form of a pine cone.

2.
 yolk sac tumor in a 65-year-old man. Surg Neurol 1994;42:253-8.

(8.) Chong SM, Wee A, Yeoh SC, et al. Retroperitoneal retroperitoneal /ret·ro·peri·to·ne·al/ (-per?i-to-ne´al) posterior to the peritoneum.

ret·ro·per·i·to·ne·al
adj.
Situated behind the peritoneum.
 endodermal sinus tumor: Report of a case with an abnormal cervicovaginal smear. Acta Cytol 1994;38:562-7.

(9.) Teilum G, cited by Kempson RL, Hendrickson MR. The female reproductive system. In: Coulson WF, ed. Surgical Pathology. Philadelphia: J.B. Lippincott, 1978:718.

(10.) Mostofi FK, Sesterhenn IA, Davis CJ Jr. Immunopathology of germ cell tumors of the testis. Semin Diagn Pathol 1987;4:320-41.

(11.) Megerian CA, McKenna MJ, Nuss RC, et al. Endolymphatic sac tumors: Histopathologic confirmation, clinical characterization, and implication in von Hippel-Lindau disease. Laryngoscope 1995;105:801-8.

(12.) Delisle MB, Urn E, Rouquette I, et al. Papillary neoplasm of the endolymphatic sac in a patient with von Hippel-Lindan disease. J Clin Pashol 1994;47:959-61.

(13.) Pollak A, Bohmer A, Spycher M, Fisch U. Are papillary adenomas endolymphatic sac tumors? Ann Otol Rhinol Laryngol 1995;104:613-9.

(14.) Gaffey MJ, Mills SE, Fechner RE, et al. Aggressive papillary middle-ear tumor: A clinicopathologic entity distinct from middle-ear adenoma. Am 3 Surg Pathol 1988;12:790-7.

(15.) Gaffey MJ, Mills SE, Boyd JC. Aggressive papillary tumor of the middle ear/temporal bone and adnexal adnexal /ad·nex·al/ (ad-nek´sal) pertaining to adnexa.

adnexal

pertaining to, or emanating from, the adnexa.


adnexal tumors
 papillary cystadenoma: Manifestations of von Hippel-Lindau disease. Am J Surg Pathol 1994; 18:1254-60.

(16.) Alford BR, Guilford FR. A comprehensive study of tumors of the glomus jugulare. Laryngoscope 1962;72:765-87.

(17.) Larson TC, Reese DF, Baker HL Jr., McDonald TJ. Glomus glomus /glo·mus/ (glo´mus) pl. glom´era   [L.]
1. a small histologically recognizable body composed of fine arterioles connecting directly with veins, and having a rich nerve supply.

2.
 tympanicum chemodectomas: Radiographic and clinical characteristics. Radiology 1987; 163:801-6.

(18.) Reddy EK, Mansfield CM, Hartman GV. Chemodectoma of the glomus jugulare. Cancer 1983;52:337-40.
                       Immunohistochemical features
Antibody          Dilution  Source   Result
Desmin            Predilute Ventana    --
Cytokeratin       Predilute Ventana   +++
S-100             Predilute Ventana    --
Glial fibrillary  1:10      Signet     --
 acidic protein
Chromogranin      1:10      BioGenex   --
Synaptophysin     1:160     Dako       --
Neuron-specific   1:8       Signet     --
 enolase
Somatostatin      1:3       Dako       --
Alpha fetoprotein 1:3       Dako       --
Vimentin          Predilute Ventana   +++
COPYRIGHT 2000 Medquest Communications, LLC
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2000, Gale Group. All rights reserved. Gale Group is a Thomson Corporation Company.

 Reader Opinion

Title:

Comment:



 

Article Details
Printer friendly Cite/link Email Feedback
Author:Subramony, Charu
Publication:Ear, Nose and Throat Journal
Article Type:Brief Article
Date:Mar 1, 2000
Words:2336
Previous Article:Spondyloepiphyseal dysplasia congenita associated with conductive hearing loss.
Next Article:Kimura's disease: A case report.
Topics:



Related Articles
Xanthoma of the temporal bone: A unique case of this rare condition.
Giant benign sinonasal squamous papilloma: Report of a case.
Incidental petrous apex findings on magnetic resonance imaging.
Diagnosis and treatment of lipomas of the internal auditory canal.
Cellular schwannoma of the paranasal sinuses: initial report of a case. (Original Article).
Plasmacytoma of the petrous temporal bone.
Giant-cell reparative granuloma of the temporal bone: a case report and review of the literature.
Obstructing lesions of the endolymphatic sac and duct mimicking Meniere's disease.
World Health Organization classification of tumours: pathology and genetics of head and neck tumours.
Extramedullary plasmacytoma of the nasal cavity: treatment perspective in a developing nation.

Terms of use | Copyright © 2014 Farlex, Inc. | Feedback | For webmasters