From Churg–Strauss Syndrome to Eosinophilic Granulomatosis With Polyangiitis: A Historical Review of Nomenclature and Diagnostic Criteria

American Journal of Dermatopathology, Год журнала: 2021, Номер 44(5), С. 315 - 320

Опубликована: Ноя. 23, 2021

Eosinophilic granulomatosis with polyangiitis (EGPA) is rare vasculitis syndrome that involves the skin and other organ systems manifesting as asthma, eosinophilia, pulmonary infiltrates. The understanding of EGPA, previously known Churg-Strauss Syndrome, has continued to evolve from its earliest documentation in literature 1951. Herein, we review key historical advances diagnosis, classification, nomenclature EGPA have shaped our this protean disorder over time.

Язык: Английский

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Case 7-2023: A 70-Year-Old Man with Covid-19, Respiratory Failure, and Rashes

New England Journal of Medicine, Год журнала: 2023, Номер 388(10), С. 926 - 937

Опубликована: Март 8, 2023

Pr esentation of C a seDr. Carolina Geadas (Medicine): A 70-year-old man with history kidney transplantation was evaluated at this hospital because multiple erythematous rashes that had developed during an admission for respiratory failure, pneumococcal bacteremia, and failure.Approximately 4.5 years before the current admission, patient received diagnosis antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis after he presented progressive glomerulonephritis failure new hemoptysis.The anti-myeloperoxidase titer 221.0 U (reference value, <2.8).The underwent plasmapheresis, cyclophosphamide prednisone were administered.Hemodialysis initiated.Two weeks later, rituximab administered, discontinued.During next 4 years, his renal function did not improve, treatment hemodialysis continued.Four months from deceased donor hepatitis virus antibody-positive status.After transplantation, immunosuppressive therapy included dose basiliximab, mycophenolate mofetil, tacrolimus, tapering doses prednisone.The delayed graft function; blood creatinine level decreased approximately 4.00 mg per deciliter (354 mmol liter) immediately to 1.50 (133 6 later.Six days routine follow-up visit, 1.33 (118 liter).Four began have central abdominal discomfort, nausea, anorexia, chills, diarrhea loose stools three times day.During several days, noticed urine output malaise, rhinorrhea, cough, sinus congestion, dyspnea.He brought emergency department hospital.

Язык: Английский

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Juvenile Temporal Arteritis with Hypereosinophilic Syndrome Masquerading as An Epidermal Inclusion Cyst of the Scalp

Indian Journal of Vascular and Endovascular Surgery, Год журнала: 2023, Номер 10(2), С. 155 - 157

Опубликована: Апрель 1, 2023

A 34-year-old man came to the outpatient department with subcutaneous nodules in temporal area. He did not complain of any other symptoms. Computed tomography scan revealed a nodule 40.5 HU region scalp. possibility an epidermal inclusion cyst was given. The lesion excised and biopsy vasculitis eosinophilia without giant cell formation. final diagnosis juvenile arteritis hypereosinophilic syndrome given based on clinical, radiological, histopathological findings.

Язык: Английский

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Optic Disk Granuloma in Eosinophilic Granulomatosis with Polyangiitis: A Case Report Illustrating the Utility of Multimodal Imaging

Ocular Immunology and Inflammation, Год журнала: 2024, Номер 32(8), С. 1910 - 1912

Опубликована: Янв. 9, 2024

Язык: Английский

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Vasculitis asociadas a los anticuerpos anticitoplasma de neutrófilos (ANCA): de la A a la Z

Piel, Год журнала: 2024, Номер 39(7), С. 416 - 427

Опубликована: Май 8, 2024

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Asymptomatic, extensive brownish macules and patches on the lower abdomen and legs

Indian Journal of Dermatology Venereology and Leprology, Год журнала: 2024, Номер 0, С. 1 - 3

Опубликована: Авг. 1, 2024

Язык: Английский

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Atypical clinical presentation of eosinophilic angiocentric fibrosis with cutaneous and upper respiratory tract involvement

Journal of Cutaneous Pathology, Год журнала: 2024, Номер 51(11), С. 821 - 824

Опубликована: Авг. 15, 2024

The authors declare no conflict of interest. Research data are not shared.

Язык: Английский

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Non-Specific Facial Oedema in a Patient with Eosinophilic Granulomatosis with Polyangiitis

Indian Journal of Dermatology, Год журнала: 2024, Номер 69(5), С. 423 - 423

Опубликована: Сен. 1, 2024

Язык: Английский

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Granulomatöse Vaskulitiden

Springer eBooks, Год журнала: 2024, Номер unknown, С. 169 - 174

Опубликована: Янв. 1, 2024

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Umbilicated papulonodules on the elbows with purpuric papules on the fingers

Clinical and Experimental Dermatology, Год журнала: 2022, Номер 47(5), С. 999 - 1002

Опубликована: Март 8, 2022

This case describes an unusual cutaneous presentation. Our patient had purpuric papules on the fingers and umbilicated nodules over elbows, interestingly, both lesion types showed similar histopathological features of necrobiotic granuloma with neutrophils.

Язык: Английский

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