Cocorullo G, Scerrino G, Melfa G, Raspanti C, Rotolo G, Mannino V, Richiusa P, Cabibi D, Giannone A G, Porrello C, Gulotta G
G Chir. 2017 Sep-Oct;38(5):243-249. doi: 10.11138/gchir/2017.38.5.243.
Parathyroid carcinoma (PC) is a very rare endocrine tumour, usually characterized by symptoms such as a neck mass, dysphonia, severe hypercalcemia exceeding 140 mg/L and elevated serum parathyroid hormone levels, even more than 5 times the upper limit of normal. Non-functioning parathyroid cancer is extremely rare and, in this case, its pre-operative diagnosis is often difficult. A 54-year old female patient, referring dysphagia and dysphonia, underwent neck ultrasound and neck CT. A left thyroid nodule, probably cystic, was found. It presented caudal extent on anterior mediastinum causing compression of the left lateral wall of the trachea. The preoperative calcemia was into the normal range. The patient underwent left thyroid lobectomy. Histological exam showed a cystic lesion, immunohistochemically originating from parathyroid that oriented for carcinoma. The 18 months follow-up did not show a residual-recurrent disease. The parathyroid origin of a neck lesion could not be suspected before surgery when specific laboratory tests are not available and clinical effects of hyperparathyroidism syndrome are not present. Histological features are not always sufficient for the differential diagnosis between the parathyroid adenoma and carcinoma. The immunohistochemistry is an useful tool that can aid to reach the definite diagnosis.
甲状旁腺癌(PC)是一种非常罕见的内分泌肿瘤,通常表现为颈部肿块、声音嘶哑、严重高钙血症(超过140mg/L)以及血清甲状旁腺激素水平升高,甚至超过正常上限的5倍等症状。无功能甲状旁腺癌极为罕见,在这种情况下,其术前诊断往往很困难。一名54岁女性患者,因吞咽困难和声音嘶哑就诊,接受了颈部超声和颈部CT检查。发现一个左侧甲状腺结节,可能为囊性,其向纵隔前部延伸,导致气管左侧壁受压。术前血钙水平在正常范围内。患者接受了左侧甲状腺叶切除术。组织学检查显示为囊性病变,免疫组化显示起源于甲状旁腺,倾向于癌。18个月的随访未显示残留或复发性疾病。当没有特定的实验室检查且不存在甲状旁腺功能亢进综合征的临床症状时,术前很难怀疑颈部病变起源于甲状旁腺。组织学特征对于甲状旁腺腺瘤和癌的鉴别诊断并不总是足够的。免疫组化是有助于做出明确诊断的有用工具。