Hyalinizing clear cell carcinoma of the head and neck: Case series and update

Albergotti, William Greer; Bilodeau, Elizabeth A.; Byrd, J. Kenneth; Mims, Mark M; Lee, Stella; Kim, Seungwon

doi:10.1002/hed.23902

Cited by 48 publications

(87 citation statements)

References 55 publications

(98 reference statements)

Supporting

Mentioning

Contrasting

Unclassified

Order By: Relevance

“…Of 153 patients with some form of clinical data reported or available, 144 underwent primary surgical resection. Lymph node dissection was reported in 26 cases, with positive nodes in 13 . Neck dissection, where specified, was usually unilateral, and limited to supraomohyoid levels I to III.…”

Section: Resultsmentioning

confidence: 99%

“…Neck dissection, where specified, was usually unilateral, and limited to supraomohyoid levels I to III. Adjuvant or neoadjuvant therapy was performed in 26 cases, including 8 patients who had also undergone lymph node dissection . Radiation was the preferred adjuvant modality in 24 cases, with combined chemotherapy/radiotherapy being administered in 2 cases.…”

Section: Resultsmentioning

confidence: 99%

“…HCCC characteristics were compared with other salivary gland carcinomas presenting to our institution using nonparametric Mann–Whitney U test for continuous variables, or Fisher exact test for dichotomous variables. Clinical outcomes of our cases combined with that of 99 reported HCCCs with available follow‐up from primary resection, were plotted using the Kaplan–Meier method. Duplicate (previously reported) cases were excluded.…”

Section: Methodsmentioning

confidence: 99%

“…Hyalinizing clear cell carcinoma (HCCC) was first characterized as a distinct salivary gland neoplasm in 1994, although descriptions of clear cell carcinomas of salivary origin are reported in the literature as far back as 1972 . Generally considered a low‐grade malignancy, HCCC may recur locoregionally, with rare distant metastases, most frequently to the lungs . Until recently, HCCC was considered to be a diagnosis of exclusion .…”

Section: Introductionmentioning

confidence: 99%

See 3 more Smart Citations

Reappraising hyalinizing clear cell carcinoma: A population‐based study with molecular confirmation

et al. 2016

View full text Add to dashboard Cite

show abstract

Section: Resultsmentioning

confidence: 99%

Section: Resultsmentioning

confidence: 99%

Section: Methodsmentioning

confidence: 99%

Section: Introductionmentioning

confidence: 99%

See 2 more Smart Citations

Reappraising hyalinizing clear cell carcinoma: A population‐based study with molecular confirmation

et al. 2016

View full text Add to dashboard Cite

show abstract

“…29, 30, 31, 32, 33 EWSR1 gene rearrangement also can be seen in extraskeletal myxoid chondrosarcoma, clear cell sarcoma, hyalinizing clear cell carcinoma, clear cell odontogenic carcinoma, desmoplastic small round cell tumor, and myxoid liposarcoma. 34, 35, 36, 37, 38, 39 Thus, corroborating morphologic, immunophenotypic, and genetic features is required for a definitive ES diagnosis.…”

Section: Discussionmentioning

confidence: 99%

Primary Ewing Family of Tumors of the Jaw Has a Better Prognosis Compared to Tumors of Extragnathic Sites

Owosho

Rosenberg

et al. 2016

Journal of Oral and Maxillofacial Surgery

View full text Add to dashboard Cite

Purpose Primary Ewing sarcoma of the jaw is rare. The aim of this study was to describe new cases of primary Ewing sarcoma of the jaw and investigate reported prognostic factors of Ewing sarcoma in this series and treatment outcome. Materials and Methods Six patients with primary Ewing sarcoma of the jaw were treated at the Memorial Sloan Kettering Cancer Center (MSKCC) from 1992 through 2013. Clinical data, pathology reports, treatment prescribed, treatment regimens, outcome, and follow-up information were reviewed. Results Five of 6 patients were female and 5 cases were in the mandible. No patient presented with metastatic disease at diagnosis. All cases were positive for CD99, and 3 patients with genetic confirmation were positive for EWS-FLI1 fusion or EWSR1 gene rearrangement. All patients received induction multiagent chemotherapy and surgical resection and 2 patients received adjuvant radiotherapy. Total (grade IV) or nearly total (grade III) tumor necrosis in 3 of 5 patients (60%) assessed for histologic response to chemotherapy indicated intense sensitivity. All patients were alive and free of disease, with no history of local recurrence, at a median follow-up period of 6.5 years. Conclusion Patients with primary Ewing sarcoma of the jaw have a good prognosis and metastasis is an uncommon occurrence at initial presentation.

show abstract

The key radiologic and cytomorphologic features of oncocytic and oncocytoid lesions of the salivary gland

Lubin

Song

Zafar

et al. 2019

Diagnostic Cytopathology

View full text Add to dashboard Cite

Oncocytic and oncocytoid lesions represent a distinct subset of salivary gland lesions. True oncocytic lesions of the salivary gland are entirely composed of oncocytes. These are characterized by the presence of abundant eosinophilic granules due to the presence of abundant cytoplasmic mitochondria. Oncocytic lesions of the salivary gland include oncocytosis, oncocytoma, and oncocytic carcinoma. In addition to the true oncocytic lesion, there exists another group of salivary gland lesions, which demonstrate cells with abundant and occasionally granular cytoplasm. These are often termed as “oncocytoid” lesions. The recently proposed Milan System for reporting salivary gland cytology clearly states that fine‐needle aspiration specimens representing oncocytic/oncocytoid lesions of salivary gland cannot effectively distinguish between a nonneoplastic lesion, benign and malignant neoplasms. Therefore, most lesions lacking classic cytomorphologic features will be classified under the umbrella diagnostic term of “Salivary Gland Neoplasm of Uncertain Malignant Potential” (SUMP). In this review, we discuss and illustrate key clinicopathologic and radiologic features that can help the practicing cytopathologist narrow down the differential and provide the best management based diagnosis.

show abstract

Hyalinizing clear cell carcinoma of the head and neck: Case series and update

Abstract: HCCC has an overall good prognosis with potential for aggressive behavior. The presence of necrosis, locoregional disease, or positive margins is associated with risk for recurrence.

Cited by 48 publications

References 55 publications

Reappraising hyalinizing clear cell carcinoma: A population‐based study with molecular confirmation

Reappraising hyalinizing clear cell carcinoma: A population‐based study with molecular confirmation

Primary Ewing Family of Tumors of the Jaw Has a Better Prognosis Compared to Tumors of Extragnathic Sites

The key radiologic and cytomorphologic features of oncocytic and oncocytoid lesions of the salivary gland

Contact Info

Product

Resources

About