The first case report of primary thyroid teratocarcinosarcoma: An analog to sinonasal teratocarcinosarcoma.

IF 0.9 Q4 ONCOLOGY Rare Tumors Pub Date : 2021-08-29 eCollection Date: 2021-01-01 DOI:10.1177/20363613211043662
Akwasi Ofori Abayie, Kofi Mensah Nyarko, Markus Bährle, Alfred Brütting
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引用次数: 3

Abstract

Teratocarcinosarcoma is a rare and aggressive tumor usually affecting the sinonasal tract. It arises primarily from the nasal cavity, paranasal sinuses with some reported cases arising from the nasopharynx and oral cavity and commonly referred to as Sinonasal Teratocarcinosarcoma (SNTC). We present the first case of teratocarcinosarcoma as a primary thyroid cancer in a 17-year-old male patient who presented with a rapidly growing anterior neck mass with no symptoms. Physical examination revealed circa 4 cm × 5 cm slightly right sided, non-tender, firm anterior neck swelling. A thyroid ultrasound revealed an enlarged thyroid gland with multiple thyroid nodes. Magnetic Resonance Imaging (MRI) of the head and neck showed no sinonasal tract tumor. Thyroidectomy and surgical resection of the tumor was performed. Histological examination revealed teratocarcinosarcoma of the thyroid gland, an analog to SNTC with no primary sinonasal tissue involvement. This implies that, teratocarcinosarcoma can occur in primary tissues other than sinonasal origin contrary to conventional knowledge.

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原发性甲状腺畸胎癌肉瘤一例报告:类似鼻窦畸胎癌肉瘤。
畸胎瘤是一种罕见的侵袭性肿瘤,通常影响鼻窦。它主要发生在鼻腔、鼻窦,有报道的病例发生在鼻咽部和口腔,通常被称为鼻窦畸形瘤肉瘤(SNTC)。我们提出第一例畸胎癌肉瘤作为原发性甲状腺癌在17岁的男性患者谁提出了快速增长的前颈部肿块无症状。体格检查显示约4厘米× 5厘米,略右侧,无压痛,颈部前部肿胀。甲状腺超声显示甲状腺肿大伴多发甲状腺结节。头颈部核磁共振检查未见鼻窦肿瘤。行甲状腺切除术及手术切除肿瘤。组织学检查显示甲状腺畸胎性癌肉瘤,类似SNTC,没有原发性鼻窦组织累及。这表明,畸胎癌肉瘤可以发生在鼻窦起源以外的原发组织,这与传统的认识相反。
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Rare Tumors
Rare Tumors ONCOLOGY-
CiteScore
1.50
自引率
0.00%
发文量
15
审稿时长
15 weeks
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