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Morphologic and Ancillary Studies of Pediatric Acinic Cell Carcinoma: A Single Institute Experience.
Cole, Grayson G; Salgado, Cláudia M; Vargas de Stefano, Danielle; Zambrano, Eduardo V; Gómez, Ana M; Reyes-Múgica, Miguel; Wang, Qian.
Afiliación
  • Cole GG; Department of Diagnostic Sciences, Oral and Maxillofacial Pathology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, PA, USA.
  • Salgado CM; Department of Pathology, University of Pittsburgh Medical Center, Children's Hospital of Pittsburgh, 4401 Penn Ave, Pittsburgh, PA, 152240, USA.
  • Vargas de Stefano D; Department of Pathology, University of Pittsburgh Medical Center, Children's Hospital of Pittsburgh, 4401 Penn Ave, Pittsburgh, PA, 152240, USA.
  • Zambrano EV; Department of Pathology, University of Pittsburgh Medical Center, Children's Hospital of Pittsburgh, 4401 Penn Ave, Pittsburgh, PA, 152240, USA.
  • Gómez AM; Department of Pathology, University of Pittsburgh Medical Center, Children's Hospital of Pittsburgh, 4401 Penn Ave, Pittsburgh, PA, 152240, USA.
  • Reyes-Múgica M; Department of Pathology, University of Pittsburgh Medical Center, Children's Hospital of Pittsburgh, 4401 Penn Ave, Pittsburgh, PA, 152240, USA.
  • Wang Q; Department of Pathology, University of Pittsburgh Medical Center, Children's Hospital of Pittsburgh, 4401 Penn Ave, Pittsburgh, PA, 152240, USA. wangq7@upmc.edu.
Head Neck Pathol ; 17(1): 204-209, 2023 Mar.
Article en En | MEDLINE | ID: mdl-36169793
ABSTRACT

BACKGROUND:

Acinic cell carcinoma (AciCC) is the second most common pediatric malignant salivary gland tumor. However, there are limited pathology publications about this tumor in the pediatric population.

METHODS:

We describe four pediatric AciCC cases diagnosed between 2000 and 2021 in our institute. Reticulin histochemistry plus immunohistochemistry for NR4A3 and DOG1 were performed on all cases.

RESULTS:

Histologically, all four cases featured a tumor-associated lymphoid proliferation and collagenous stroma, in which two formed central scars. The tumors were predominantly solid, with a lobular pattern and variably sized dilated spaces, including one case with focal microcysts. High-grade transformation was not observed in any of our cases. Reticulin stain and immunohistochemistry for NR4A3 showed distinct features between AciCC and non-neoplastic salivary gland parenchyma. DOG1 immunohistochemistry confirmed the acinar origin of AciCC.

CONCLUSIONS:

Our study reveals that pediatric AciCCs often present with tumor-associated lymphoid proliferation (TALP) and sclerosis. Special stains such as reticulin histochemistry and NR4A3 immunohistochemistry are helpful to separate tumor from adjacent benign parenchyma. The ancillary study is helpful for the diagnosis of small specimens. Our study is limited by its low case number, but we hope that our results will promote more studies on this rare salivary gland tumor in the pediatric population.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias de las Glándulas Salivales / Carcinoma de Células Acinares Límite: Child / Humans Idioma: En Revista: Head Neck Pathol Asunto de la revista: NEOPLASIAS / PATOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias de las Glándulas Salivales / Carcinoma de Células Acinares Límite: Child / Humans Idioma: En Revista: Head Neck Pathol Asunto de la revista: NEOPLASIAS / PATOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos
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