Publications by authors named "Sameera Husain"

Article Synopsis
  • Lichen sclerosus et atrophicus (LSA) is a chronic skin condition primarily affecting female genitalia, while morphea is a rare inflammatory skin disorder characterized by hard skin patches.
  • There is an ongoing debate among researchers about whether LSA and morphea are related or separate conditions, particularly when they occur in the same patient.
  • A case is reported involving a 62-year-old woman with both extragenital LSA-morphea overlap in her inguinal folds and subsequent development of genital LSA three months later, highlighting the rare progression between these two conditions that had not been previously documented.
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Article Synopsis
  • Angioleiomyoma is a benign tumor made of smooth muscle cells found in blood vessels, commonly appearing as a painful lump under the skin, especially in the lower legs of middle-aged women.
  • It is a rare type of tumor in the foot, making preoperative diagnosis quite uncommon.
  • The text discusses a specific case of a 28-year-old woman with angioleiomyoma in her ankle, emphasizing the need for early and accurate diagnosis to differentiate it from potentially harmful tumors like leiomyosarcoma.
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A male in his 60s developed a pruritic, maculopapular rash on his torso and arms, sparing his palms and soles. He tested positive for ANA and an initial skin biopsy identified "bullous lupus," supporting the diagnosis of a connective tissue disease. Additional symptoms included headaches, facial nerve palsy and hearing loss, which partially responded to oral corticosteroids.

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BRAF/MEK inhibition remains standard of care for treatment of BRAF-mutated non-small cell lung cancer (NSCLC). Although common adverse events (AEs) have been reported through clinical trials and ongoing clinical practice, only a handful of reports have detailed unusual adverse events associated with these medications. This report presents a patient with BRAF-mutated NSCLC treated with dabrafenib and trametinib who experienced 2 unusual AEs-Sweet syndrome and MEK-associated retinopathy-that responded to steroid treatment.

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Significance: Hemolacria (bloody tears) is a rare clinical presentation with varied underlying etiologies. Thorough clinical evaluation is essential to diagnosis and management.

Purpose: This study aimed to report unilateral hemolacria in a known contact lens wearer with an occult, palpebral, conjunctival pyogenic granuloma and review the literature.

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Continuous subcutaneous insulin infusion (CSII), or insulin pumps, with or without continuous glucose monitoring (CGM) devices have become the standard of care for patients with type 1 diabetes. While increasingly popular, a wide range of reported skin reactions to CSII and CGM devices was found. We present this case of a pyogenic granuloma-like neutrophilic and granulomatous response to an insulin pump to increase awareness of a previously uncharacterized cutaneous adverse reaction at insulin pump infusion sites.

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The association between Henoch-Schönlein purpura (HSP) and neoplasia is rare and has been more commonly reported in cases of solid tumors rather than hemotological malignancies. To the authors' knowledge, HSP in association with orbital lymphoma has not been previously reported. An 84-year-old man underwent anterior orbitotomy with biopsy for a rapidly growing orbital mass.

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Lymphomatoid papulosis (LyP) is a paraneoplastic primary cutaneous CD30 lymphoproliferative disorder (LPD) that has been associated with malignant lymphomas, most commonly mycosis fungoides (MF). We observed 10 patients with MF who developed severe inflammation after using nitrogen-mustard (NM) gel from 1 to 8 months and who developed LyP. We hypothesized that NM gel produced local inflammation, which induced CD30 expression in malignant T cells in situ leading to the appearance of LyP papules.

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Article Synopsis
  • The study aims to explore the unknown causes of infantile hemangiomas (IH) and related syndromes (PHACE and LUMBAR), focusing on histopathologic features of midline anomalies in patients.
  • Researchers conducted a review of 18 midline lesions from 13 patients with IH, noting various histopathologic diagnoses, including several types of hamartomas and other lesions.
  • The findings suggest a link between PHACE syndrome and rhabdomyomatous mesenchymal hamartoma, which may offer insights into the developmental issues causing IH and related syndromes.
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