Publications by authors named "Magro C"

Background: Microvascular thrombosis is key to the pathogenesis of calciphylaxis. C5b-9-mediated microvascular injury reflective of complement pathway activation could be a key pathophysiologic event.

Methods: We conducted a retrospective multicenter study of 24 patients who have had biopsy-supported calciphylaxis from the 2010-2022 data base from Emory where C5b-9 immunohistochemistry (IHC) had not been conducted and the 2019-2023 data base from Cornell where C5b-9 IHC was done as part of the routine calciphylaxis work up.

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Pyoderma gangrenosum (PG) is a rare necrotizing neutrophilic dermatosis driven by monokines and cytokines elaborated by monocytes and autoreactive T cells, respectively. Th1-mediated autoimmune disorders and myeloproliferative disease are among the potential disease associations. More recently, certain medications were implicated, including TNF-alpha inhibitors, rituximab, and IL-17A inhibitors, such as secukinumab, where the development of PG is held to represent a cutaneous immune adverse effect.

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  • Systemic arterial properties play a crucial role in determining clinical outcomes and variations in patients with degenerative calcific aortic stenosis (AS), yet many previous studies overlooked pulsatile pressure-flow relations as a critical assessment method.
  • A retrospective study of 135 AS patients examined the relationship between pulsatile load and risk of mortality and heart failure hospital admissions using advanced modeling techniques.
  • Results show that pressure-dependent total arterial compliance is a significant predictor of mortality and adverse heart failure events, outperforming traditional measures of arterial load, suggesting that understanding arterial wall pressure can better identify high-risk patients.
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  • Various systemic diseases can show abnormalities on a normal skin biopsy, which can assist in making accurate diagnoses, especially for conditions like thrombotic microvascular diseases and dysautonomia syndromes.
  • A review of skin biopsy data revealed specific patterns and markers that are linked to certain diseases, including increased C5b-9 deposition and signaling changes related to interferon.
  • The findings emphasize that skin biopsies provide valuable insights into multi-organ diseases, highlighting their importance in clinical evaluations.
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  • Malignant atrophic papulosis, also known as Köhlmeier-Degos disease, was first identified in 1941 and is characterized by skin rashes and serious intestinal issues, including perforations.
  • This disease involves unique vascular damage affecting microvasculature and arteries, leading to distinctive skin lesions and changes in blood vessel structure.
  • A case study highlights the emergence of Köhlmeier-Degos disease following treatment with a TNF-alpha inhibitor (golimumab), exploring the relationship between TNF-alpha and type I interferon signaling in the disease's progression.
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Background: The prevalence of cardiovascular disease is burgeoning in low- and middle-income countries (LMICs). In sub-Saharan Africa, the prevalence of cardiovascular risk factors is increasing, though rates of CVD diagnosis and management remain low. Awareness of the influence of social determinants of health (SDOH) on cardiovascular outcomes is growing, however, most work focuses on high-income countries.

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  • An 82-year-old woman with a history of vocal cord paralysis and rheumatoid arthritis presented to the emergency department with symptoms including shortness of breath, chest tightness, and coughing up blood for the past month.
  • Despite multiple courses of antibiotics as an outpatient, her condition did not improve.
  • Due to potential risk for airway complications, she was subsequently admitted to the hospital for further treatment.
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  • Researchers investigated cases of lymphoproliferative disorders (LPDs) and cutaneous lymphomas that appeared after COVID-19 vaccination, examining the link between specific vaccines and these reactions.
  • They found 50 biopsy-proven cases primarily from the U.S., Italy, and Greece, with the Pfizer-BioNTech vaccine associated with 72% of these instances.
  • Most patients experienced favorable outcomes, with a common form being lymphomatoid papulosis, and treatment options varied from observational care to medication like steroids and methotrexate.
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Background: Segmental aplasia of the caudal vena cava (CVC) with azygos continuation is a congenital malformation macroscopically described in mammals including humans, dogs, and rodents. It is usually detected as an incidental finding and the final diagnosis is reached by computed tomography (CT), fluoroscopy, or post-mortem dissection.

Case Description: A 3-year-old guinea pig () presented with subacute dyspnea.

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  • Onychopapilloma typically shows up as longitudinal redness under the nail, but its diagnosis can be tricky due to varying symptoms, with most patients experiencing functional issues rather than pain.
  • A case study presented a 74-year-old woman who had splitting and sensitivity in her right thumbnail for five years, with clinical tests and X-rays showing no significant findings, leading to a nail biopsy.
  • The biopsy revealed onychopapilloma along with a rare concurrent traumatic neuroma, highlighting the need for biopsy for accurate diagnosis and suggesting a broader range of conditions to consider when dealing with painful nails.
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Tebentafusp is a bispecific protein that recently underwent FDA approval for the treatment of metastatic uveal melanoma that functions by redirecting cytotoxic T cells to glycoprotein-100, a protein highly expressed in melanoma. Although clinical trials have demonstrated that rashes are common in the first few days of treatment, little is known about skin reactions that develop later in the treatment course. Herein, we describe a type IV hypersensitivity reaction and vitiligo-like depigmentation that developed six weeks into treatment and discuss the possible mechanisms underlying these reactions.

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  • Mucha-Habermann disease (MHD) is an inflammatory skin condition with symptoms resembling cutaneous T-cell lymphoma, while its severe variant, febrile ulceronecrotic MHD (FUMHD), presents with systemic symptoms and ulcers.
  • A case study of a 21-year-old woman showed atypical lymphomatoid features of FUMHD alongside hemophagocytic lymphohistiocytosis (HLH), leading to significant clinical findings and a biopsy that indicated atypical CD8 + lymphocyte infiltration.
  • Treatment using etoposide and dexamethasone resulted in rapid improvement of her symptoms, with the patient's skin lesions healing over time and confirming the MHD diagnosis; she has remained
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  • Skin ulcers can be difficult to diagnose, especially when they are related to other health issues like autoimmune and gastrointestinal diseases, and simple explanations might not always apply.
  • A case involving a 70-year-old male revealed that what was thought to be a skin condition related to Crohn's disease was actually basal cell carcinoma, which worsened and led to amputation.
  • The key takeaway is to always reassess a diagnosis and consider getting more expert opinions when a patient's condition doesn't improve, as earlier diagnosis could have prevented severe outcomes.
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T cell dyscrasias that demonstrate a proclivity for the subcutaneous fat include atypical lymphocytic lobular panniculitis, lupus profundus, and primary subcutaneous T cell lymphoma, including subcutaneous panniculitis-like T cell lymphoma (SPTCL). We encountered two patients who developed fever and indurated abdominal erythema at their peginterferon alfa-2a injection sites. Biopsies showed an atypical CD8 positive, granzyme positive, CD5 negative, MXA negative lymphocytic lobular panniculitis, diagnostic of SPTCL.

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Cereal grains serve as the cornerstone of global nutrition, providing a significant portion of humanity's caloric requirements. However, the presence of fungal genera, such , , , and , known for their mycotoxin-producing abilities, presents a significant threat to human health due to the adverse effects of these toxins. The primary objective of this study was to identify the predominant fungal contaminants in cereal grains utilized in breadmaking, as well as in flour and bread.

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A 16-year-old adolescent boy presented with recurrent episodes of weakness and numbness. Brain MRI demonstrated subcortical, juxtacortical, and periventricular white matter T2 hyperintensities with gadolinium enhancement. CSF was positive for oligoclonal bands that were not present in serum.

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Background And Objectives: TEMPI (telangiectasias, elevated erythropoietin and erythrocytosis, monoclonal gammopathy, perinephric fluid collections, and intrapulmonaryshunting) syndrome is a rare multisystemic disease classified as a monoclonal gammopathy of cutaneous significance. The pathogenesis and etiology of TEMPIare not well known because of the rarity of this disorder. Although telangiectasias are the hallmark of this syndrome, skin biopsies are rarely performed.

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