Publications by authors named "Raja Seethala"

Article Synopsis
  • Molecular studies indicate that ALT is a crucial prognostic marker for shorter relapse-free survival (RFS) in pancreatic neuroendocrine tumors (PanNETs) and other neoplasms.
  • The development of a new chromogenic ALT assay (ALT-CISH) was initiated to address clinical limitations of the traditional fluorescence in situ hybridization (FISH) method, showing a 100% agreement with FISH results in validating that ALT is present in 31% of primary PanNETs.
  • The study demonstrated that ALT status is significantly associated with poorer RFS in both PanNET and leiomyosarcoma (LMS) patients, with ALT being an independent prognostic factor
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Sialadenoma papilliferum is a tumor characterized by surface papillary projections and glandular/microcystic proliferation at the lesion base. Cases in which surface involvement is absent have been termed "sialadenoma papilliferum-like intraductal papillary tumor." Similar tumors that are present in the mandible have been termed "tubulopapillary hidradenoma-like tumor of the mandible.

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  • Accurate staging for nasopharyngeal carcinoma (NPC) is vital for treatment and prognosis, using the AJCC/UICC TNM system as a standardized approach, necessitating ongoing updates to reflect modern care practices.
  • The study aimed to enhance the accuracy and relevance of the TNM-8 system for NPC by analyzing patient data from 2014-2015 and undergoing rigorous validation processes leading to the development of TNM-9.
  • Results from over 4,900 patients highlighted that advanced extranodal extension was a key negative prognostic factor, prompting a proposed restructuring of staging for nonmetastatic cases from TNM-8 classifications.
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  • Kürsteiner canals (KC) are embryological remnants linked to parathyroid and thymic development, with ongoing research aimed at understanding their role in various parathyroid lesions and cysts.
  • A study evaluated 62 cystic and 22 non-cystic parathyroid lesions over a 12-year period, identifying distinct KC phenotypes in relation to the presence of parathyroid hormone (PTH).
  • The findings reveal that KC commonly appear in parathyroids, particularly in non-PTH cysts, and suggest that these manifestations may originate from KC, while PTH-positive cysts are associated with different characteristics.
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Introduction: Thyroid cytopathology cases with suspicious for malignancy (SFM) diagnosis often result in resection. However, molecular testing offers details that may provide additional insights. In this study, the molecular profiles of SFM cases from two institutions that routinely used ThyroSeq v3 (TSV3) were examined.

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  • Detection of extranodal extension (ENE) in head and neck squamous cell carcinoma indicates a poor prognosis, but there's currently a lack of standardized diagnostic criteria and reporting methods in the literature.
  • The Head and Neck Cancer International Group organized a modified Delphi process involving 19 pathology experts to establish consensus recommendations for diagnosing and reporting ENE.
  • The resulting guidelines, supported by 19 organizations from 34 countries, aim to standardize the diagnosis and improve accuracy in data collection regarding histology detected extranodal extension.
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Background: MYB RNA in situ hybridization (ISH) has emerged as a reliable and accessible marker to support adenoid cystic carcinoma (ACC) diagnosis, though still not well studied. Here, we report our results in a validation and prospective cohort to improve MYB RNA ISH diagnostic accuracy.

Methods: 79 cases (23 retrospective and 56 prospective) underwent MYB RNA ISH testing (44 ACC and 35 non-ACC).

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Article Synopsis
  • - NIFTP is a newly classified thyroid neoplasm that has replaced the previous diagnosis of a certain type of thyroid cancer, with varying adoption rates noted across different global regions.
  • - A survey of 48 pathologists showed a 94% adoption rate for diagnosing NIFTP, with North American pathologists diagnosing it more frequently than those in Europe and Asia/Oceania.
  • - Significant differences exist in how pathologists assess nuclear features, especially for moderate changes, leading to regional variations in NIFTP diagnosis, with North American and European pathologists generally using lower thresholds for diagnosis compared to their counterparts in Asia/Oceania.
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While acinic cell carcinoma (AciCC) can undergo high-grade transformation (HGT) to high-grade adenocarcinoma or poorly differentiated carcinoma, other morphologies such as spindle cell/sarcomatoid carcinoma are rare and not well-characterized. We herein report a novel case of AciCC with squamoglandular and chondrosarcomatous HGT mimicking a so-called 'carcinosarcoma ex-pleomorphic adenoma'. The patient is an 81-year-old male with a two-month history of neck swelling and referred otalgia who presented with a left parapharyngeal space mass extending into retropharyngeal space and pterygoid muscles.

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Context.—: High-grade transformation, previously known as dedifferentiation, in salivary gland carcinoma and carcinosarcoma ex pleomorphic adenoma is a rare phenomenon. It is, however, clinically relevant and affects treatment and prognosis.

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Context.—: Biomarker reporting has increasingly become a key component of pathology reporting, providing diagnostic, prognostic, and actionable therapeutic data for patient care.

Objective.

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Biphenotypic sinonasal sarcoma (BSNS) is a rare neoplasm of the sinonasal tract. These tumors show neural and myogenic differentiation and are characterized by translocations. The immunophenotypic features reflect their dual differentiation.

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Article Synopsis
  • The study investigates how molecular tests, like ThyroSeq v3, can help assess risks of malignancy in indeterminate thyroid cytopathology cases, providing a more accurate risk probability compared to traditional methods.
  • Results showed that molecular-derived risk of malignancy (MDROM) rates for various cytopathologic diagnoses were generally within established reference ranges, but the positive call rates (PCR) varied more significantly among cytopathologists, particularly for atypia of undetermined significance (AUS).
  • The findings suggest that MDROMs and PCRs can serve as valuable metrics for evaluating cytopathologists’ performance and improving overall quality in diagnosing thyroid conditions.
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Anaplastic thyroid carcinoma (ATC) demonstrates a wide variety of morphologies and is characteristically associated with a differentiated thyroid carcinoma component. Heterologous differentiation is a rare, potentially challenging phenomenon in ATC, mostly observed as osteosarcomatous or chondrosarcomatous differentiation. We now describe a novel 'glomangiosarcoma-like' differentiation, review our archival experience from two institutions (UPMC, CC), and perform a systematic review for the prevalence of heterologous elements in ATC.

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Context.—: Salivary gland tumors are rare tumor types for which the molecular understanding has resulted in a rapid expansion and shuffling of entities. These changes are reflected in the 5th edition World Health Organization Classification of Head and Neck Tumours (WHO 5th edition), although many nuances still remain.

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Article Synopsis
  • A 67-year-old female with a history of chronic lymphocytic leukemia presented with painful swelling in her right parotid gland, which was diagnosed as acinic cell carcinoma (AciCC) after a biopsy.
  • Imaging revealed metastatic lung nodules confirming the spread of AciCC, leading to extensive surgical intervention that included a radical parotidectomy and neck dissection.
  • The tumor exhibited specific histological features, strong immunohistochemical reactivity, and electron microscopy findings, supporting the classification of AciCC, while concurrent CLL/SLL was found in lymph nodes without tumor involvement.
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Sclerotic fibroma (SF) is an uncommon yet benign tumor that may occasionally be associated with Cowden's disease that presents as an asymptomatic, well-circumscribed lesion. We present a rare case of a patient with a solitary SF of the palpebral conjunctiva. The patient was an 85-year-old male who presented with a right lower lid nodule that was initially treated as a chalazion.

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Background: Odontogenic carcinosarcoma (OCS) is a rare odontogenic malignancy with limited characterization and unexplored molecular features. We report clinicopathologic and molecular findings in 3 additional OCS and review the literature.

Methods: 3 OCS (5.

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 Olfactory neuroblastoma (ONB), or esthesioneuroblastoma, is a rare neuroectodermal tumor of the nasal cavity and paranasal sinuses. Most of these tumors express somatostatin receptors (SSTRs), providing a potential target for radionuclide imaging with Ga-68 DOTATATE. However, this imaging modality has not been extensively studied in ONB.

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Background: Lymphadenomas are rare benign tumors of the major salivary glands that are further classified as sebaceous and non-sebaceous. No association with viruses has been reported so far. Little is known about the mechanisms that allow lymphadenomas to undergo malignant transformation.

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Background: Secretory myoepithelial carcinomas (SMCA) are rare, mucinous, signet ring predominant tumors with primitive myoepithelial features. While many mucinous salivary gland tumors have now been molecularly characterized, key drivers in SMCA have yet to be elucidated. Recently, NKX3.

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Introduction: Indeterminate thyroid cytology diagnoses are associated with intermediate risks of malignancy. Application of molecular testing (MT) to indeterminate specimens provides additional diagnostic and prognostic information. While a positive or suspicious MT result may prompt surgery, a negative MT result is associated with a low probability of cancer or noninvasive follicular thyroid neoplasm with papillary-like nuclear features and approximates that of a benign cytology diagnosis.

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