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Extragonadal teratomas of the adult abdomen and pelvis: a pictorial review
Authors:E J O'Donovan  K Thway  E C Moskovic
Institution:The Royal Marsden NHS Trust, London, UK
Abstract:Teratomas comprise a spectrum of tumours that have striking imaging appearances and are commonly considered when evaluating a mass in the female pelvis. A subgroup of these tumours located in an extragonadal abdominopelvic location, in contrast, are extremely rare and can affect both sexes. Extragonadal teratomas can occur at all ages, are particularly unusual in adults and can cause confusion in the differential diagnosis, especially in children. Familiarity with the imaging features of the spectrum of teratomas within the abdominal cavity is therefore of great importance, as radiological diagnosis can guide treatment, prevent delays in diagnosis and avoid sequelae. This article summarizes the radiological appearances of these rare extragonadal tumours in adults in relation to their pathology, malignant potential, location and behaviour. Although uncommon, teratomas should be considered in the differential diagnosis of extragonadal abdominal masses, particularly in young adults.Teratomas are neoplasms with tissue components resembling normal derivatives of the three germ layers. They comprise a spectrum of tumours with striking imaging appearances and are commonly considered when evaluating pelvic masses in females. Extragonadal abdominopelvic teratomas are, in contrast, very rare and are seen in both sexes. They represent only 1–5% of germ cell tumours (GCTs)1 and therefore may not be readily considered by clinicians. Their radiological appearances are, however, characteristic, and familiarity with these features will lead to more accurate radiological diagnoses that not only guide treatment but also prevent avoidable complications from diagnostic delay.Teratomas can present at any age. They contain tissue elements foreign to the organ or anatomic site of origin.2 Arising from totipotent germ cells, they contain derivatives of one to all three germ cell layers (the ectoderm, endoderm and mesoderm)24 and occur most frequently in the ovary or testis. Gonadal teratomas are well described; however, the extragonadal variants are under-represented in the literature. These encompass mature cystic teratomas (MCTs), which are most frequently tridermal lineage, and epidermoid cysts, which are frequently classified pathologically as monodermal teratomas (MTs) (
LineageTumour
Bi-/tridermalMature cystic/benign teratoma
Bi-/tridermalImmature teratoma (containing immature neural/neuroectodermal tissue)
Bi-/tridermalMalignant (teratoma plus malignant foci)
MonodermalEpidermoid cyst
MonodermalStruma ovarii
Open in a separate windowHistologically, both MCT (Figure 1a) and MT (Figure 1b) are lined by squamous epithelium but MTs lack skin appendageal structures. Postulated theories for the extragonadal location of teratomas include origin from displaced germ cells during embryologic migration,1 ectopic ovarian tissue and ovarian dermoids reimplanting in an extragonadal site.3Open in a separate windowFigure 1.(a) Photomicrograph of mature cystic teratoma with a fibrous wall lined by keratinizing stratified squamous epithelium (bottom right of field). The wall contains skin appendageal structures, including sebaceous follicles (arrow), a hair follicle (thin arrow) and arrector pili muscle bundles (thick arrow). (b) Photomicrograph of monodermal teratoma with a fibrous tissue wall of the cyst (thin arrow), lined by mature, keratinizing stratified squamous epithelium (arrow). Keratin flakes and keratinous debris are present within the lumen (thick arrow).
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