2020
DOI: 10.1016/j.joms.2019.11.008
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Castleman Disease of the Parotid Gland: A Case Report

Abstract: Castleman disease is a rare lymphoproliferative disorder characterized by the formation of painless hyperplastic lymph nodes. It can affect any lymph nodes of the body but rarely affects the salivary gland. We describe a patient with unicentric Castleman disease presenting as a parotid tumor and discuss the diagnosis and treatment of Castleman disease. A 39-year-old man had a painless lump on the right side of his face for 1 year. A computed tomography scan showed a well-defined, homogeneous mass in the right … Show more

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Cited by 6 publications
(10 citation statements)
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“…Two forms of the disease are recognised, unicentric and multicentric (MCD), with the latter often being associated with immunosuppression and HHV8 infection. Microscopically, two subtypes are identified: the more common hyaline vascular variant and the plasma cell variant 22–24 . The plasma cell variant may be further subdivided to include HHV8‐positive and HHV8‐negative cases.…”
Section: Hhv8‐associated Lymphoproliferative Disorders In Immunosuppressed Patientsmentioning
confidence: 99%
See 2 more Smart Citations
“…Two forms of the disease are recognised, unicentric and multicentric (MCD), with the latter often being associated with immunosuppression and HHV8 infection. Microscopically, two subtypes are identified: the more common hyaline vascular variant and the plasma cell variant 22–24 . The plasma cell variant may be further subdivided to include HHV8‐positive and HHV8‐negative cases.…”
Section: Hhv8‐associated Lymphoproliferative Disorders In Immunosuppressed Patientsmentioning
confidence: 99%
“…Lymphadenopathy is the main clinical finding, with B symptoms (fever, night sweats and weight loss) reported in over 95% of patients. Other common clinical presentations include splenomegaly and hepatomegaly 22,23 …”
Section: Hhv8‐associated Lymphoproliferative Disorders In Immunosuppressed Patientsmentioning
confidence: 99%
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“…So, certain diagnosis is essential to avoid unnecessary treatment. The diagnosis of CD is challengeable for clinicians and pathology evaluation is requirement to affordable treatment [ 6 ]. The clinical symptoms and signs are various and the diagnosis is problematic and optimal managing is still indefinite.…”
Section: Introductionmentioning
confidence: 99%
“…Rarely, unicentric Castleman disease presents in unusual sites, including the lung, pancreas, liver, adrenal, orbits, nasopharynx, spleen, parotid gland, and small bowel. [2][3][4][5][6][7][8][9][10] It has no specific clinical or radiologic features. Histologic examination is the key to a correct diagnosis.…”
mentioning
confidence: 99%