| Literature DB >> 28924477 |
Alex González Bóssolo1, Michelle Mangual Garcia2, Paula Jeffs González3, Miosotis Garcia1, Guillermo Villarmarzo3, Jose Hernán Martinez1.
Abstract
Classical papillary thyroid microcarcinoma (PTMC) is a variant of papillary thyroid carcinoma (PTC) known to have excellent prognosis. It has a mortality of 0.3%, even in the presence of distance metastasis. The latest American Thyroid Association guidelines state that although lobectomy is acceptable, active surveillance can be considered in the appropriate setting. We present the case of a 37-year-old female with a history of PTMC who underwent surgical management consisting of a total thyroidectomy. Although she has remained disease-free, her quality of life has been greatly affected by the sequelae of this procedure. This case serves as an excellent example of how first-line surgical treatment may result more harmful than the disease itself. LEARNING POINTS: Papillary thyroid microcarcinoma (PTMC) has an excellent prognosis with a mortality of less than 1% even with the presence of distant metastases.Active surveillance is a reasonable management approach for appropriately selected patients.Patients should be thoroughly oriented about the risks and benefits of active surveillance vs immediate surgical treatment. This discussion should include the sequelae of surgery and potential impact on quality of life, especially in the younger population.More studies are needed for stratification of PTMC behavior to determine if conservative management is adequate for all patients with this specific disease variant.Entities:
Year: 2017 PMID: 28924477 PMCID: PMC5592700 DOI: 10.1530/EDM-17-0065
Source DB: PubMed Journal: Endocrinol Diabetes Metab Case Rep ISSN: 2052-0573
Figure 1(A) (x400 H&E stain) The neoplastic follicles are lined by cells with variation in size, that are haphazardly arranged and show nuclear clearing, irregular contour, nuclear grooves and intranuclear pseudoinclusions (arrow) and uneven spacing of the nuclei in the neoplastic follicle, which are the characteristic changes of papillary thyroid carcinoma; (B) x40 Hematoxylin and Eosin (H&E) stain demonstrates the unencapsulated nature of the tumor. (*) Shows the fibrous septa dividing the neoplastic epithelium. The tumor also presents an infiltrative border with a predominantly follicular architecture and occasional papilla (arrow) seen. The right-side area represents benign thyroid parenchyma composed of macro follicles filled with colloid (pink proteinaceous material), and small blue follicular cells; the neoplastic epithelium shows nuclear clearing and less amount of colloid characteristic of thyroid carcinoma; and (C) (x100 H&E stain) This figure shows at the center, the characteristic well-formed papillae of the neoplastic follicular cells and the absence of colloid. The upper left side (*) demonstrate the lymphoid infiltrate characteristic of lymphocytic (Hashimoto’s) thyroiditis; composed of lymphocytes (small dark blue cells) forming the mantle zone and the central area composed of more oncocytic cells (histiocytes) admixed with lymphocytes.
Active surveillance trials for papillary microcarcinoma.
| Author (year) | Country | Follow-up (years) | ||||
|---|---|---|---|---|---|---|
| Ito | Japan | 340 | 10 | 3.4 | 0 | 0 |
| Sugitani | Japan | 230 | 5 | 1 | 0 | 0 |
| Ito | Japan | 1235 | 10 | 3.8 | 0 | 0 |
| Hitomi | Japan | 1179 | 3 | 0.5 | 0 | 0 |
| Kwon | Korea | 192 | 3.5 | 4 | 0 | 0 |
N/A: Not available.
Retrospective analysis.
Unfavorable events after thyroid surgery of low-risk PTMC (15).
| Transient vocal cord paralysis | 0.6% | 4.1% | <0.0001 |
| Transient hypoparathyroidism | 2.8% | 16% | <0.0001 |
| Permanent hypothyroidism | 0.08% | 1.6% | <0.0001 |
| Post-surgical hematoma | 0% | 0.5% | <0.05 |
Guidelines recommendation regarding papillary thyroid microcarcinoma management.
| American Thyroid Association (ATA) (2015) | ‘Could be considered’ | Recommended if history of radiation, familial carcinoma and cervical nodal metastases | Recommended if no ETE and N0 |
| Korean Thyroid Association (KTA) (2016)* | Will adopt the recommendation | Recommended if history of radiation, familial carcinoma and cervical nodal metastases | Recommended if no ETE and N0 |
| British Thyroid Association (2014) | No recommendation stated | Recommended if multifocality | Recommended if no other risk factors** |
| National Comprehensive Cancer Network (NCCN) (2017) ( | No recommendation stated | Recommended for high risk patients*** | Recommended for low-risk patients**** |
| AACE/ACE-AME (2016) ( | ‘May be acceptable’ | Surgical approach is based on preoperative imaging and the clinical setting | Surgical approach is based on preoperative imaging and the clinical setting |
Official statement not yet published; **Risk factors: Size (6–10 mm) multifocal extrathyroidal extension poorly differentiated; ***High risk: tumor more than 4 cm, ETE, multifocal, nodal metastases, confirmed contralateral disease, or vascular invasion; ****Low risk: negative resection margins, no contralateral lesion, no suspicious lymph node(s), and small (<1 cm).
ETE, Extrathyroidal extension; N0, No lymph node involvement; AACE/ACE-AME, American College of Clinical Endocrinologists, American College of Endocrinology, Associazione Medici Endocrinologi.