Postoperative pancytopenia in a patient with giant parathyroid adenoma and brown tumor: a case report.

IF 2.8 3区 医学 Q3 ENDOCRINOLOGY & METABOLISM BMC Endocrine Disorders Pub Date : 2024-09-30 DOI:10.1186/s12902-024-01742-x
Wen-Ting Pan, Zhi-Hong Zhao, Kun Wang, Zhi-Yuan He, Liang Ou
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Abstract

Background: Parathyroid adenoma is the primary cause of primary hyperparathyroidism, commonly presenting with elevated parathyroid hormone (PTH) and blood calcium levels. Chronic primary hyperparathyroidism often results in bone destruction, resulting in the formation of brown tumors. The preferred clinical treatment for parathyroid adenoma is parathyroidectomy. Postoperative pancytopenia, although rare, is a critical complication that warrants further investigation into its mechanisms and management strategies.

Case presentation: We present a case of a 59-year-old female patient who was admitted due to nausea and vomiting. Positron emission tomography-computed tomography (PET-CT) revealed a mass posterior to the left thyroid lobe and multiple areas of fibrocystic osteitis throughout the body. Hematological tests showed elevated serum calcium and parathyroid hormone (PTH) levels. The patient subsequently underwent parathyroidectomy, and pathological examination confirmed the presence of a parathyroid adenoma. Postoperatively, the patient developed pancytopenia and received symptomatic treatment such as correction of anemia and elevation of white blood. At the two-month follow-up, all indicators had returned to normal.

Conclusions: Pancytopenia is commonly seen in bone marrow diseases, infections and immune-related disorders, nutritional deficiencies, and metabolic diseases. This case confirms that pancytopenia can also occur postoperatively in patients with parathyroid adenoma. Therefore, Clinicians should be aware of the potential for postoperative pancytopenia following parathyroidectomy and the need for prompt management.

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一名患有巨大甲状旁腺腺瘤和棕色瘤的患者术后出现全血细胞减少:病例报告。
背景:甲状旁腺腺瘤是原发性甲状旁腺功能亢进症的主要病因,通常表现为甲状旁腺激素(PTH)和血钙水平升高。慢性原发性甲状旁腺功能亢进通常会导致骨质破坏,形成褐色肿瘤。甲状旁腺腺瘤的首选临床治疗方法是甲状旁腺切除术。术后全血细胞减少虽然罕见,但却是一种严重的并发症,需要进一步研究其机制和治疗策略:我们介绍了一例 59 岁的女性患者,她因恶心和呕吐入院。正电子发射计算机断层扫描(PET-CT)显示左甲状腺叶后方有肿块,全身多处有纤维囊性骨炎。血液学检查显示血清钙和甲状旁腺激素(PTH)水平升高。患者随后接受了甲状旁腺切除术,病理检查证实了甲状旁腺腺瘤的存在。术后,患者出现全血细胞减少,接受了纠正贫血和升高白细胞等对症治疗。在两个月的随访中,所有指标均恢复正常:全血细胞减少症常见于骨髓疾病、感染和免疫相关疾病、营养缺乏和代谢性疾病。本病例证实,甲状旁腺腺瘤患者术后也可能出现全血细胞减少。因此,临床医生应意识到甲状旁腺切除术后可能会出现全血细胞减少的情况,并需要及时处理。
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来源期刊
BMC Endocrine Disorders
BMC Endocrine Disorders ENDOCRINOLOGY & METABOLISM-
CiteScore
4.40
自引率
0.00%
发文量
280
审稿时长
>12 weeks
期刊介绍: BMC Endocrine Disorders is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of endocrine disorders, as well as related molecular genetics, pathophysiology, and epidemiology.
期刊最新文献
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