Results 101 to 110 of about 24,507 (317)

Multiple Bilateral Erythematous and Suppurative Cutaneous Nodules in a 40‐Year‐Old Indian Female

JEADV Clinical Practice, EarlyView.
Aditi Anand, Shaivy Malik, Charanjeet Ahluwalia   +2 more
wiley   +1 more source

Acute-onset, painful, acral granuloma annulare in a 52-year-old female

JAAD Case Reports, 2022
Faisal S. Ahmad, BA, Michael R. Vittori, MD, William H. McCoy, 4th, MD, PhD   +2 more
doaj   +1 more source

Meningeal Relapse of Nodular Lymphocyte Predominant Hodgkin Lymphoma Transformed to T-Cell/Histiocyte-Rich Large B-Cell Lymphoma: A Case Report

Frontiers in Oncology, 2020
Central nervous system involvement in Hodgkin lymphoma is extremely rare, especially in nodular lymphocyte predominant Hodgkin lymphoma (NLPHL), which usually carries a favorable prognosis.
Paolo Salvioni Chiabotti, Bettina Bisig, Anne Cairoli, Steven D. Hajdu, Pierre-Yves Lovey, Dina Milowich, Sonia Ziadi, Renaud Du Pasquier, Jean-Philippe Brouland, Laurence de Leval   +9 more
doaj   +1 more source

Longstanding Perianal Ulcers

JEADV Clinical Practice, EarlyView.
Narachai Julanon, Thanaphon Anutraungkool, Sirawich Jessadapattarakul, Vincent Piguet   +3 more
wiley   +1 more source

DIFFUSION NORMOLIPIDEMIC FLAT XANTHOMA, ASSOCIATED WITH HYPOCHROMIC ANEMIA. DESCRIPTION OF THE CASES

Vestnik Dermatologii i Venerologii, 2017
The diffuse plane xanthoma (DPX) belongs to the class II of histiocytosis arising from the dermal dendritic cells (Histiocyte Society). The dominate role in the formation of the disease in the skin plays an accumulation of phagocytic immune complexes of ...
V. D. Elkin, T. G. Sedova, E. V. Plotnikova, I. D. Kuznetsov, M. U. Novoselova   +4 more
doaj   +1 more source

Adult-onset Still's disease: Evaluation of prognostic tools and validation of the systemic score by analysis of 100 cases from three centers [PDF]

, 2016
Background: Adult-onset Still's disease (AOSD) is rare inflammatory disease of unknown etiology that usually affects young adults. The more common clinical manifestations are spiking fevers, arthritis, evanescent rash, elevated liver enzymes ...
Berardicurti O., Carubbi F., Ciccia F., Cipriani P., Di Benedetto P., Giacomelli R., Guggino G., Iacono D., Liakouli V., Masedu F., Ruscitti P., Triolo G., Valenti M., Valentini G.   +13 more
core   +1 more source

Analysis of pathological features of lymph node in adult-onset Still disease

Zhongguo Linchuang Yixue
ObjectiveTo summarize the pathological morphological features, diagnosis, and differential diagnosis of adult-onset Still disease (AOSD), and to improve clinical understanding of the disease.
Ting CHEN, Yingyong HOU, Xiaowen GE
doaj   +1 more source

Hemophagocytic lymphohistiocytosis presenting with acute liver failure and central nervous system involvement in early infancy

Indian Journal of Pathology and Microbiology, 2018
Hemophagocytic lymphohistiocytosis (HLH) is a potentially fatal and likely underdiagnosed disease characterized by unregulated histiocyte proliferation, hypercytokinemia and hemophagocytosis, causing life-threatening tissue damage and organ failure.
Mukesh Kumar, Nirupama Kothari, B D Gupta, Neeraj Gupta   +3 more
doaj   +1 more source

Histiocytic sarcoma simulating immune thrombocytopenic purpura [PDF]

, 2012
published_or_final_versio
Hwang, YY, Kwong, YL, Leung, RYY, Sim, PYJ, So, JCC   +4 more
core   +2 more sources

Bilateral Periareolar Nodules in an Adolescent With a History of Lymphoma

JEADV Clinical Practice, EarlyView.
Rawan Almutairi, Mohamed Saad, Hamad Alajmi, Ali Alajmi, Humoud Al‐Sabah, Atlal Allafi   +5 more
wiley   +1 more source