Histoid Neoplasm

Histoid neoplasm is a rare type of malignant tumor that typically affects skin, subcutaneous tissue and lymph nodes. It is characterized by its distinctive histological pattern, which is composed of small interlacing cords and glands. Histoid neoplasm can spread locally or metastasize to other parts of the body, making it difficult to treat. However, when diagnosed early and treated appropriately, prognosis is often favorable. Due to its rarity, histoid neoplasm is often included as part of a more inclusive diagnosis of lymphoma or sarcoma of unknown origin. Histoid neoplasm is important to study and diagnose, as it provides essential information on the biology of malignant tumors, allowing physicians to provide better treatment plans.

← Journal of Neoplasms

Related Articles

6 article(s) found

First Evidences of Epithelial-Mesenchymal Transition and Cancer Stem-Cell Phenotype Acquisition in Dermo-Epidermal Junction of BPV-Infected Neoplasms

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Newly-Detected Solitary Bony Lytic/Sclerotic Lesion with Soft Tissue Mass in a Previously Treated Case of High-Risk Medulloblastoma: Importance of Contemporary Pathology Techniques to Differentiate Second Malignant Neoplasm from Extra-Neuraxial Metastasis 

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Changes in Statistics of Malignant Neoplasms of Central Nervous System Excluding Brain (ICD-10: C70, C72) In the Lower Silesia Region of Poland in the Years 2006-2012

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Statistical Analysis of Malignant Brain Neoplasms (ICD-10: C71) in the Lower Silesia Region of Poland in the Years 2006-2012

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Rare Lipomatous Neoplasm of The Thigh in A 13 Year Old Male with A Discussion of Imaging Features and Differential Diagnosis of A Fatty Extremity Mass

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A Case Report on Challenging Management of Multiple Neoplasms in Elderly

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