Clavicle metastasis from carcinoma thyroid- an atypical skeletal event and a management dilemma
Arvind Krishnamurthy
Abstract:Bone metastases is a well described event in the natural history of thyroid cancers and has the potential to severely impact the quality of life by causing pain, fractures and spinal cord compression. Follicular thyroid carcinomas have a greater propensity for distal metastasis than papillary and anaplastic thyroid carcinomas. The most common sites of skeletal metastasis among thyroid cancer patients are femur followed by humerus, pelvis, radius, and scapula. Clavicle metastasis at initial presentation is exce… Show more
“…While bone metastases are rare, they can manifest as a complication of aggressive thyroid carcinoma [ 3 ]. Bone has been reported as the second most common metastasis site with well-differentiated thyroid cancer, with follicular carcinoma more prevalent as an etiology (7–28%) than that of PTC origin (1.4–7%) [ 9 , 11 ]. To this end, our case depicts a unique presentation of thyroidal tissue metastases to the bone due to being confirmed a papillary subtype of well-differentiated thyroid cancer, which typically has a very low propensity for bone metastasis.…”
Section: Discussionmentioning
confidence: 99%
“…However, the clavicle's scarce red marrow and scant vascularity make it a rare location for malignancy [ 15 ]. As a result, metastatic involvement of the clavicle becomes an even more rare event (0–15% of all known clavicular lesions) with little known about its management [ 9 ]. Most presentations of clavicular lesions are reported in small case studies with a broad spectrum of presentations [ 16 ].…”
Section: Discussionmentioning
confidence: 99%
“…While the lung is considered the most common site of metastases from thyroid malignancy, bone metastases, if seen, are usually observed at skeletal sites such as the humerus, pelvis, radius, and scapula. PTC metastases to the clavicular bone as an initial presentation is a rare and unique finding [ 9 ]. We present a case of PTC that was first noticed as a growth on the right base of the neck and later found to have metastasized to the right clavicle.…”
Objective. We present the case of a 44-year-old man with a large neck mass to highlight the unique presentation of papillary thyroid carcinoma (PTC) metastatic to the clavicle. Methods. We reviewed the medical record for a detailed history and physical examination findings. Our radiology colleagues examined the diagnostic imaging studies performed. The pathology team reviewed the neck mass biopsy and the confirmatory surgical pathology after total resection of the mass. Results. A 44-year-old man presented with an enlarging neck mass. Initial X-rays revealed a large soft tissue density mass that extended to the midline of the right clavicle. A neck ultrasound established a 5.4 × 3.6 cm mass with increased vascularity and calcification extending from the thyroid. A CT scan noted the extension of the mass into the adjacent sternoclavicular junction with osteolysis of the middle third of the clavicle and the superior aspect of the sternal body. Fine-needle aspiration revealed a thyroid neoplasm with follicular features and positive immunostaining consistent with thyroid carcinoma. The patient underwent a composite resection of the tumor, including a segmental osteotomy of approximately two-thirds of the medial clavicle. The pathology report confirmed PTC with extrathyroidal extension and clavicle involvement (staged pT4a pN0), with further genomic findings showing positive KRAS mutation. Conclusion. Clavicular metastasis from differentiated thyroid cancer is rare. While the prognosis is generally favorable, various factors, including age greater than 45 years, poor differentiation, follicular thyroid carcinoma, Hurthle cell variant, and extrapulmonary metastasis, have typically been associated with poorer cancer-specific survival.
“…While bone metastases are rare, they can manifest as a complication of aggressive thyroid carcinoma [ 3 ]. Bone has been reported as the second most common metastasis site with well-differentiated thyroid cancer, with follicular carcinoma more prevalent as an etiology (7–28%) than that of PTC origin (1.4–7%) [ 9 , 11 ]. To this end, our case depicts a unique presentation of thyroidal tissue metastases to the bone due to being confirmed a papillary subtype of well-differentiated thyroid cancer, which typically has a very low propensity for bone metastasis.…”
Section: Discussionmentioning
confidence: 99%
“…However, the clavicle's scarce red marrow and scant vascularity make it a rare location for malignancy [ 15 ]. As a result, metastatic involvement of the clavicle becomes an even more rare event (0–15% of all known clavicular lesions) with little known about its management [ 9 ]. Most presentations of clavicular lesions are reported in small case studies with a broad spectrum of presentations [ 16 ].…”
Section: Discussionmentioning
confidence: 99%
“…While the lung is considered the most common site of metastases from thyroid malignancy, bone metastases, if seen, are usually observed at skeletal sites such as the humerus, pelvis, radius, and scapula. PTC metastases to the clavicular bone as an initial presentation is a rare and unique finding [ 9 ]. We present a case of PTC that was first noticed as a growth on the right base of the neck and later found to have metastasized to the right clavicle.…”
Objective. We present the case of a 44-year-old man with a large neck mass to highlight the unique presentation of papillary thyroid carcinoma (PTC) metastatic to the clavicle. Methods. We reviewed the medical record for a detailed history and physical examination findings. Our radiology colleagues examined the diagnostic imaging studies performed. The pathology team reviewed the neck mass biopsy and the confirmatory surgical pathology after total resection of the mass. Results. A 44-year-old man presented with an enlarging neck mass. Initial X-rays revealed a large soft tissue density mass that extended to the midline of the right clavicle. A neck ultrasound established a 5.4 × 3.6 cm mass with increased vascularity and calcification extending from the thyroid. A CT scan noted the extension of the mass into the adjacent sternoclavicular junction with osteolysis of the middle third of the clavicle and the superior aspect of the sternal body. Fine-needle aspiration revealed a thyroid neoplasm with follicular features and positive immunostaining consistent with thyroid carcinoma. The patient underwent a composite resection of the tumor, including a segmental osteotomy of approximately two-thirds of the medial clavicle. The pathology report confirmed PTC with extrathyroidal extension and clavicle involvement (staged pT4a pN0), with further genomic findings showing positive KRAS mutation. Conclusion. Clavicular metastasis from differentiated thyroid cancer is rare. While the prognosis is generally favorable, various factors, including age greater than 45 years, poor differentiation, follicular thyroid carcinoma, Hurthle cell variant, and extrapulmonary metastasis, have typically been associated with poorer cancer-specific survival.
“…Apart from the rare site of metastasis from differentiated thyroid cancer, the case also illustrates the fact that small volume metastatic skeletal disease at times can demonstrate an excellent response to 131 I therapy. [ 1 2 3 4 5 ]…”
Rare solitary metacarpophalangeal skeletal metastasis from poorly differentiated carcinoma of thyroid is reported in this communication. The case demonstrated excellent tumor marker and scan response to two fractions of radioiodine therapy (serum thyroglobulin 0.01 ng/ml at the time of the 3rd follow-up) and is being presently followed up on levothyroxine suppression.
Objectives
Our discussant’s thoughtful consideration of the patient’s case allows for review of three maxims of medicine: Occam’s razor (the simplest diagnosis is the most likely to be correct), Hickam’s dictum (multiple disease entities are more likely than one), and Crabtree’s bludgeon (the tendency to make data fit to an explanation we hold dear).
Case presentation
A 66-year-old woman with a history of hypertension presented to our hospital one day after arrival to the United States from Guinea with chronic daily vomiting, unintentional weight loss and progressive shoulder pain. Her labs are notable for renal failure, nephrotic range proteinuria and normocytic anemia while her shoulder X-ray shows osseous resorption in the lateral right clavicle. Multiple myeloma became the team’s working diagnosis; however, a subsequent shoulder biopsy was consistent with follicular thyroid carcinoma. Imaging suggested the patient’s renal failure was more likely a result of a chronic, unrelated process.
Conclusions
It is tempting to bludgeon diagnostic possibilities into Occam’s razor. Presumption that a patient’s signs and symptoms are connected by one disease process often puts us at a cognitive advantage. However, atypical presentations, multiple disease processes, and unique populations often lend themselves more to Hickam’s dictum than to Occam’s razor. Diagnostic aids include performing a metacognitive checklist, engaging analytic thinking, and acknowledging the imperfections of these axioms.
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