Publications by authors named "Jasmine S Saleh"

Article Synopsis
  • Pleomorphic dermal sarcoma (PDS) is a rare skin tumor with similarities to atypical fibroxanthoma (AFX), but exhibits more aggressive traits.
  • PDS tends to invade deeper tissues, leading to higher risks of metastasis and local recurrence compared to AFX.
  • The review emphasizes the importance of early detection and treatment to improve patient outcomes, while summarizing the tumor's features, prognosis, and management options.
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Article Synopsis
  • Cutaneous T-cell lymphomas are rare and varied skin cancers that require teamwork among dermatologists, pathologists, and hematologists/oncologists for accurate diagnosis.
  • The article covers common types like mycosis fungoides, Sézary syndrome, and CD30+ T-cell disorders, emphasizing their clinical and histopathologic traits, as well as the challenges in distinguishing them from reactive conditions.
  • It also addresses recent updates in diagnostic classification, prognosis, treatment approaches, and the importance of accurate categorization for effective patient outcomes.
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Malakoplakia is a rare chronic inflammatory condition that most commonly involves the urogenital tract. Cutaneous malakoplakia is extremely rare and many patients diagnosed with skin involvement are immunosuppressed. While the clinical presentation of cutaneous malakoplakia is variable, the histopathologic features are quite distinct and include sheets of closely packed dermal histiocytes with foamy-appearing cytoplasm and Michaelis-Gutmann bodies that are positive with certain immunohistochemical stains.

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Context.—: Hypertrophic lichen planus (HLP) is a variant of lichen planus that can be difficult to diagnose based on histopathologic features alone. Thus, patient clinical history and clinicopathologic correlation are essential considerations to make the correct diagnosis.

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Cutaneous T-cell lymphomas are an heterogeneous group of uncommon lymphoid neoplasms that are challenging to diagnose and require close collaboration between dermatologists, pathologists and hematologists/oncologists. This article reviews the most common cutaneous T-cell lymphomas: mycosis fungoides (both classic and variant forms) as well as its leukemic counterpart Sézary syndrome, CD30+ T-cell lymphoproliferative disorders including the ever-expanding group of lymphomatoid papulosis and primary cutaneous anaplastic large cell lymphoma, and primary cutaneous CD4+ small/medium lymphoproliferative disorder. We discuss the classic clinical and histopathologic features of these lymphomas and review how they can be distinguished from reactive entities.

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Article Synopsis
  • Cutaneous vascular tumors are a diverse group of skin growths that can be difficult to diagnose due to their similar appearance and features.
  • Advances in research have led to better classification and understanding of these tumors, especially through efforts by the International Society for the Study of Vascular Anomalies (ISSVA).
  • This review article summarizes the updated information on the clinical, histopathological, and immunohistochemical traits of various cutaneous vascular tumors, as well as the genetic mutations linked to them.
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Mesenchymal tumours with melanocytic expression can pose a diagnostic challenge because they frequently demonstrate both morphological and immunohistochemical overlap with other cutaneous melanocytic neoplasms. Therefore, they present potential pathological pitfalls that may lead to a misdiagnosis of malignant melanoma. Mesenchymal neoplasms that closely mimic melanoma include malignant melanotic nerve sheath tumour (melanotic schwannoma), epithelioid schwannoma, malignant peripheral nerve sheath, cutaneous syncytial myoepithelioma, clear cell sarcoma of soft tissue, and perivascular epithelioid cell tumour.

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