Sweet syndrome with pulmonary involvement in a patient with myelodysplastic syndrome [PDF]
, 2020 We report a patient with Sweet syndrome involving the pulmonary system in the context of myelodysplastic syndrome. Although Sweet syndrome may involve a variety of organ systems, the pulmonary system is rarely affected and can result in poor clinical ...
Bordelon, Jenna +7 more
core
Autoinflammatory diseases: Update on classification diagnosis and management [PDF]
, 2017 The spectrum of systemic autoinflammatory disorders broadens continually. In part, this is due to the more widespread application of massive parallel sequencing, helping with novel gene discovery in this and other areas of rare diseases.
McDermott, MF, Pathak, S, Savic, S
core +1 more source
Pyoderma gangrenosum associated with pseudo-PelgerHuët anomaly in a patient with idiopathic myelofibrosis [PDF]
, 2022 Pseudo-Pelger-Huët anomaly is a condition in which almost all the granulocytes are hyposegmented and/or hypogranulated. It is typically recognized in peripheral blood smears and represents a marker of several disorders, such as myeloproliferative ...
Antonio Furci +5 more
core +1 more source
Genetic diagnosis of α1-antitrypsin deficiency using DNA from buccal swab and serum samples [PDF]
, 2017 Background: α1-Antitrypsin deficiency (AATD) is associated with a high risk of developing lung and liver disease. Despite being one of the most common hereditary disorders worldwide, AATD remains under-diagnosed and prolonged delays in diagnosis are ...
Barrecheguren, Miriam +5 more
core +1 more source
Neutrophilic Panniculitis: Algorithmic Approach to a Heterogeneous Group of Disorders [PDF]
Archives of Pathology & Laboratory Medicine, 2014 Context.—Neutrophilic panniculitis encompasses an etiologically and morphologically heterogeneous group of disorders. Correct histopathologic diagnosis is important in identifying certain systemic diseases and guiding appropriate treatment.Objective.—To review the clinical and histopathologic features of different types of neutrophilic panniculitis ...
openaire +2 more sources
Cutaneous polyarteritis nodosa [PDF]
, 2002 Classic polyarteritis nodosa (PAN) is a segmentary leucocytoclastic vasculitis that affects small- and medium-sized arteries. In 1931, Lindberg (Acta Med Scand 1931; 76: 183-225) described the existence of a cutaneous variant of PAN, without visceral ...
Bauza, A. (Ana) +2 more
core +1 more source
Erythema nodosum - a review of an uncommon panniculitis [PDF]
, 2014 Panniculitis, inflammation of the subcutaneous fat, is a relatively uncommon condition that usually presents with inflammatory nodules or plaques. Erythema nodosum (EN) is clinically the most frequent form of panniculitis and is considered a reactive ...
Blake, Tristan +2 more
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Immunotherapy‐Related Cutaneous Toxicities in Melanoma: A Dermoscopic Perspective
JEADV Clinical Practice, EarlyView.Dermoscopy serves as a valuable tool in the everyday dermatological and oncological practice for melanoma patients, allowing for the prompt identification of immune‐related cutaneous toxicities and guiding clinicians toward appropriate therapeutic decisions.
Grażyna Kamińska‐Winciorek +3 more
wiley +1 more source
Neutrophilic dermatoses with acute myeloid leukemia associated with an increase of serum colony-stimulating factor [PDF]
, 2008 ArticleJOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY.
Ito, T +3 more
core +3 more sources
The 2021 EULAR and ACR points to consider for diagnosis and management of autoinflammatory type I interferonopathies: CANDLE/PRAAS, SAVI and AGS [PDF]
, 2022 Objective: Autoinflammatory type I interferonopathies, chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature/proteasome-associated autoinflammatory syndrome (CANDLE/PRAAS), stimulator of interferon genes (STING)-associated ...
Adang, Laura A +31 more
core +5 more sources