Van de Kerkhof Jasmine, Bijnens Jacqueline, De Geeter Frank, Dick Catherine, De Paepe Pascale, Van den Bruel Annick
Department of ENT, H&N Surgery, General Hospital Sint-Jan, Bruges, Belgium.
Department of Nuclear Medicine, General Hospital Sint-Jan, Bruges, Belgium.
Endocrinol Diabetes Metab Case Rep. 2023 Dec 8;2023(4). doi: 10.1530/EDM-22-0385. Print 2023 Oct 1.
Primary hyperparathyroidism most commonly presents with hypercalcaemia. Rarely, parathyroid apoplexy or haemorrhage mimicking a thyroid bleeding cyst is the first presentation of a parathyroid adenoma. A woman presented with a sudden-onset painful 'goitre'. Ultrasound showed a cystic nodule located posterior to rather than in the right thyroid lobe, suggesting parathyroid adenoma bleeding. Biochemistry showed mild primary hyperparathyroidism. 99mTc-pertechnetate/sestamibi showed no uptake in the nodule, which was interpreted as a cold thyroid nodule. 18F-fluorocholine PET/CT showed uptake in the nodule, suggestive of a parathyroid adenoma. Persistent mild primary hyperparathyroidism complicated by nephrolithiasis and osteopenia favoured parathyroidectomy over a wait-and-see approach. The patient was referred for parathyroidectomy along with right thyroid lobectomy. Pathology showed an adenoma, with an eccentrically located cystic structure filled with red blood cells surrounded by a thickened fibrous capsule. In conclusion, cervical pain/haemorrhage with hypercalcaemia points to the diagnosis of parathyroid apoplexy, mimicking a thyroid bleeding cyst. Workup with ultrasound and, if available, 18F-choline PET/CT allows for timely surgery, minimizing the risk of recurrent and severe bleeding.
A bleeding cyst may be located posterior to rather than in the thyroid, suggesting a parathyroid haemorrhage. Neck pain and/or haemorrhage along with primary hyperparathyroidism point to parathyroid apoplexy. A two-step presentation has been described, with a first phase of local symptoms to be followed by visible and possibly life-threatening compressing bleeding. Therefore, an expedited workup is needed, allowing for timely surgery.
原发性甲状旁腺功能亢进最常见的表现是高钙血症。甲状旁腺卒中或出血模拟甲状腺出血性囊肿的情况极为罕见,却是甲状旁腺腺瘤的首发表现。一名女性患者出现突发疼痛性“甲状腺肿”。超声显示一个囊性结节位于右甲状腺叶后方而非内部,提示甲状旁腺腺瘤出血。生化检查显示轻度原发性甲状旁腺功能亢进。99m锝高锝酸盐/甲氧基异丁基异腈显像显示该结节无摄取,被解释为冷甲状腺结节。18F - 氟胆碱PET/CT显示该结节有摄取,提示甲状旁腺腺瘤。持续性轻度原发性甲状旁腺功能亢进并伴有肾结石和骨质减少,与观察等待相比,更倾向于甲状旁腺切除术。该患者被转诊进行甲状旁腺切除术及右甲状腺叶切除术。病理显示为腺瘤,有一个偏心性的囊性结构,充满红细胞,周围是增厚的纤维性包膜。总之,伴有高钙血症的颈部疼痛/出血提示甲状旁腺卒中的诊断,类似于甲状腺出血性囊肿。超声检查以及(如有条件)18F - 胆碱PET/CT检查有助于及时手术,将复发和严重出血的风险降至最低。
出血性囊肿可能位于甲状腺后方而非甲状腺内,提示甲状旁腺出血。颈部疼痛和/或出血以及原发性甲状旁腺功能亢进提示甲状旁腺卒中。已描述了一种两步表现,第一阶段为局部症状,随后是可见的、可能危及生命的压迫性出血。因此,需要加快检查,以便及时进行手术。