Krupinova Julia, Kim Ekaterina, Eremkina Anna, Urusova Lilia, Voronkova Iya, Slaschuk Konstantin, Dobreva Ekaterina, Mokrysheva Natalia
Department of the Parathyroid Glands Pathology and Mineral Metabolism Disorders, Endocrinology Research Centre, Dmitriya Ulianova Street, 11, 117036 Moscow, Russia.
Department of Pathology, Endocrinology Research Centre, Dmitriya Ulianova Street, 11, 117036 Moscow, Russia.
J Pers Med. 2023 Mar 19;13(3):548. doi: 10.3390/jpm13030548.
Parathyroid cancer is a rare, clinically aggressive malignancy with a prevalence of approximately 0.005% relative to all carcinoma cases and 1-5% among patients with primary hyperparathyroidism. Prognosis largely depends on the extent of the primary surgery. Non-radical surgical treatment increases the risk of local and distant metastases of the parathyroid cancer associated with limited treatment options. The combination of thyroid and parathyroid disorders has been described rather well for the general population; however, cases of parathyroid and thyroid carcinoma in the same patient are extremely rare (1 case per 3000 patients with parathyroid disorders). We present a rare clinical case of combination of parathyroid and thyroid cancers with metastases of both tumors to the neck lymph nodes in a woman with a mutation in the 1 gene (NM_130799.2): c.658T > C p.Trp220Arg (W220R), who has been exposed to radiation for 20 years before diagnosis of thyroid cancer and received renal replacement therapy with long-term hemodialysis before the diagnosis of parathyroid cancer. The patient underwent several surgeries because of metastases of the parathyroid cancer in the neck lymph nodes. Surgeons used intraoperative navigation methods (single-channel gamma detection probe, Gamma Probe 2, and fluorescence angiography with indocyanine green (ICG)) to clarify the volume of surgery. Currently, the patient is still in laboratory remission, despite the structural recurrence of tumors.
甲状旁腺癌是一种罕见的、具有临床侵袭性的恶性肿瘤,在所有癌症病例中的患病率约为0.005%,在原发性甲状旁腺功能亢进患者中占1%-5%。预后很大程度上取决于初次手术的范围。非根治性手术治疗会增加甲状旁腺癌局部和远处转移的风险,且治疗选择有限。甲状腺和甲状旁腺疾病的合并情况在普通人群中已有较为充分的描述;然而,同一患者同时患有甲状旁腺癌和甲状腺癌的病例极为罕见(每3000例甲状旁腺疾病患者中有1例)。我们报告了一例罕见的临床病例,一名患有1号基因(NM_130799.2)突变:c.658T > C p.Trp220Arg(W220R)的女性,同时患有甲状旁腺癌和甲状腺癌,且两种肿瘤均转移至颈部淋巴结,该患者在诊断甲状腺癌前曾接受20年的辐射暴露,在诊断甲状旁腺癌前接受了长期血液透析的肾脏替代治疗。由于甲状旁腺癌转移至颈部淋巴结,该患者接受了多次手术。外科医生使用术中导航方法(单通道伽马探测探头、伽马探头2以及吲哚菁绿(ICG)荧光血管造影)来明确手术范围。目前,尽管肿瘤出现了结构复发,但患者仍处于实验室缓解状态。