A special case of intramedullary teratoma in an adult. Literature review

E. Ariñez Barahona , J.L. Navarro Olvera , M.A. Esqueda Liquidano , A. Muñoz Cobos , K.E. González Echeverria , A.D. Rivera Arroyo , E. Gómez Apo , R.S. Torres Durán , A. Méndez Viveros
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引用次数: 7

Abstract

Spinal teratomas that occur in adulthood are rare. The most accepted theory is that of a disembryogenic origin, but in this case we present the theory of misplaced germ cells.

We present a 54-year-old male with saddle hypoesthesia, 3/5 paraesthesia of the lower extremities, urinary incontinence, loss of anal sphincter tone, and patellar and achilles hyporeflexia, of 10 months’ evolution. The MRI showed a heterogeneous, cystic and solid intramedullary lesion with defined edges. Laminoplasty surgery of L2 to L4 and complete resection of the lesion was performed. The histopathological study found a mature teratoma.

The incidence of intraspinal teratomas is very low. There are two theories: the disembryogenic theory (most accepted) and the misplaced germ cell theory (our case). This pathogenesis of teratoma formation involves a niche of pluripotent cells from the primitive knot or a caudal cell mass that may precede the formation of a dysraphism. In this modified theory, teratoma growth sometimes causes disruption of the development field and dysraphism.

成人髓内畸胎瘤一例。文献综述
脊柱畸胎瘤发生在成年期是罕见的。最被接受的理论是去胚性起源,但在这种情况下,我们提出了错位生殖细胞的理论。我们报告一名54岁男性患者,其鞍型感觉减退,3/5下肢感觉异常,尿失禁,肛门括约肌张力丧失,髌骨和跟腱反射减退,病程10个月。MRI显示一不均匀、囊性实性髓内病变,边缘清晰。进行L2至L4椎板成形术并完全切除病变。组织病理学检查发现成熟畸胎瘤。椎管内畸胎瘤的发生率很低。有两种理论:去胚胎说(最被接受的)和错位生殖细胞说(我们的案例)。畸胎瘤形成的发病机制涉及来自原始结或尾端细胞团的多能细胞龛,可能先于畸形形成。在这个修正的理论中,畸胎瘤的生长有时会导致发育领域的破坏和发育障碍。
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来源期刊
自引率
0.00%
发文量
25
审稿时长
20 weeks
期刊介绍: The Medical Journal of the Hospital General de Mexico is the official organ of the Medical Society of the Hospital General de Mexico. The journal accepts articles in Spanish or in English on the field of hospital medicine. The journal publishes original articles, clinical cases, reviews articles, history notes, issues on medical education, short communications and editorials at the invitation of the Society. All articles are double blind peer reviewed by at least 2 reviewers and finally classified as accepted or rejected by the Editorial Board.
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