Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2020 Oct 6;8(19):4681-4687.
doi: 10.12998/wjcc.v8.i19.4681.

Parathyroid adenoma combined with a rib tumor as the primary disease: A case report

Affiliations
Case Reports

Parathyroid adenoma combined with a rib tumor as the primary disease: A case report

Lu Han et al. World J Clin Cases. .

Abstract

Background: Parathyroid adenoma is a benign parathyroid tumor, with serum parathyroid hormone and calcium ion concentrations as the typical basis for diagnosis. Its clinical manifestations are complex and changeable; thus it is easily missed or misdiagnosed. Approximately 85% of patients with parathyroid adenoma develop primary hyperparathyroidism, and abnormalities in bones, kidneys and other organs can occur. Brown tumors are rare.

Case summary: We report a rare case of fibrocystic osteitis associated with a parathyroid adenoma, which was discovered by chance due to a rib tumor. Abnormally elevated serum parathyroid hormone and calcium ion were found before surgery. We suspected primary hyperparathyroidism, and color Doppler ultrasound suggested the presence of a thyroid mass. With informed consent by the patient and her family, we first removed the rib tumor, and one week later, resection of the parathyroid adenoma and thyroid mass was performed on both sides, and the patient recovered well after surgery.

Conclusion: In the case of parathyroid adenoma combined with brown tumor, the bone cyst will gradually decrease in size with time without treatment. If not, surgery should be performed as soon as possible.

Keywords: Brown tumor; Case report; Operation; Parathyroid adenoma; Primary hyperparathyroidism; Rib; Treatment.

PubMed Disclaimer

Conflict of interest statement

Conflict-of-interest statement: The authors declare that they have no conflicts of interest to disclose.

Figures

Figure 1
Figure 1
Chest X-ray and computed tomography before surgery.
Figure 2
Figure 2
Ultrasound image of the thyroid.
Figure 3
Figure 3
Chest X-ray after surgery.
Figure 4
Figure 4
Pathological results of the rib tumor. A solid section of the cut surface, bleeding and bloody fluid are seen in the cyst cavity, fibrous tissue hyperplasia around the cystic cavity, reactive hyperplasia of bone-like tissue and trabecular bone in the deep cystic cavity, solid part of the area containing hemosiderin deposition, and multinucleated giant cell reaction.
Figure 5
Figure 5
Pathological results of the parathyroid adenoma. Left lower parathyroid gland combined with HE morphology and immunohistochemistry results diagnosis: parathyroid adenoma. Immunohistochemical results: CgA part (+), PTH (+), Ki67 (marker of proliferation Ki-67) approximately 1% (+), TG (-), and TTF-1 (thyroid transcription factor 1) (-).

Similar articles

Cited by

References

    1. Sutbeyaz Y, Yoruk O, Bilen H, Gursan N. Primary hyperparathyroidism presenting as a palatal and mandibular brown tumor. J Craniofac Surg. 2009;20:2101–2104. - PubMed
    1. Silva BC, Cusano NE, Bilezikian JP. Primary hyperparathyroidism. Best Pract Res Clin Endocrinol Metab. 2018;32:593–607. - PubMed
    1. Aresta C, Passeri E, Corbetta S. Symptomatic Hypercalcemia in Patients with Primary Hyperparathyroidism Is Associated with Severity of Disease, Polypharmacy, and Comorbidity. Int J Endocrinol. 2019;2019:7617254. - PMC - PubMed
    1. Minisola S, Gianotti L, Bhadada S, Silverberg SJ. Classical complications of primary hyperparathyroidism. Best Pract Res Clin Endocrinol Metab. 2018;32:791–803. - PubMed
    1. Marx SJ. Hyperparathyroid and hypoparathyroid disorders. N Engl J Med. 2000;343:1863–1875. - PubMed

Publication types