Results 21 to 30 of about 44,640 (263)

Demonstration of early functional compromise of bone marrow derived hematopoietic progenitor cells during bovine neonatal pancytopenia through in vitro culture of bone marrow biopsies [PDF]

, 2012
Background Bovine neonatal pancytopenia (BNP) is a syndrome characterised by thrombocytopenia associated with marked bone marrow destruction in calves, widely reported since 2007 in several European countries and since 2011 in New Zealand. The disease is
Ballingall, Keith T, Bell, Charlotte, Connelly, Maira, Dagleish, Mark P, Laming, Eleanor, Melzi, Eleonora, Rocchi, Mara S, Scholes, Sandra F E, Willoughby, Kim   +8 more
core   +2 more sources

Macrophage Activation Syndrome as Onset of Systemic Lupus Erythematosus: A Case Report and a Review of the Literature [PDF]

, 2015
Macrophage activation syndrome (MAS) is a potentially fatal condition. It is a rare complication of several autoimmune disorders, including systemic lupus erythematosus (SLE) and systemic juvenile idiopathic arthritis (sJIA).
Didona, Dario, Feola, Aldo, Granata, Guido, Granata, Massimo, Stifano, Giuseppina   +4 more
core   +4 more sources

PANCYTOPENIA;

The Professional Medical Journal, 2014
Background: Pancytopenia is an important hematological problem encounteredin our day-to-day clinical practice. The aim of our study was to evaluate clinical features andetiological pattern of pancytopenia at tertiary care settings in Abbottabad.
Atif Sitwat Hayat, Abdul Haque Khan, Ghulam Hussian Baloch, Naila Shaikh   +3 more
openaire   +2 more sources

Anorexia nervosa-associated pancytopenia mimicking idiopathic aplastic anemia: a case report

BMC Psychiatry, 2018
Background Patients with anorexia nervosa (AN) often present with pancytopenia. In most cases described in the literature, AN with pancytopenia demonstrates gelatinous marrow transformation (GMT), which is a typical bone marrow feature of malnutrition ...
Masahiro Takeshima, Hiroyasu Ishikawa, Akihiro Kitadate, Ryo Sasaki, Takahiro Kobayashi, Hiroshi Nanjyo, Takashi Kanbayashi, Tetsuo Shimizu   +7 more
doaj   +1 more source

A clinico-hematological evaluation of pancytopenia at government medical college and hospital, latur: A 2-year observational study

Medical Journal of Dr. D.Y. Patil Vidyapeeth, 2021
Context: Pancytopenia is defined by reduction of all the three formed elements of blood below the normal reference. Hematological investigation forms the bedrock in the management of patients with pancytopenia and therefore needs detailed study.
Rahul Suryakant Abhange, Rahul Pundalik Jadhav   +1 more
doaj   +1 more source

Clonal karyotype evolution involving ring chromosome 1 with myelodysplastic syndrome subtype RAEB-t progressing into acute leukemia [PDF]

, 2006
s Karyotypic evolution is a well-known phenomenon in patients with malignant hernatological disorders during disease progression. We describe a 50-year-old male patient who had originally presented with pancytopenia in October 1992.
Bennett JM, Bettina Wunderlich, Brigitte Poleck-Dehlin, Chen Z, Christoph Schmid, Cutler CS, De Witte T, Depil S, Georg Ledderose, Gisselsson D, Gullingsrud EO, Hans Jochen Kolb, Hebart H, Helga Schmetzer, Hoffmann WK, Hoffmeister PA, Holler E, Johann Mittermüller, Johansson B, Jotterand M, Kern W, Kolb HJ, Kolb HJ, Massenkeil G, Mattano, Mhawesch P, Mittermuller J, Moss PA, Mufti GJ, Rothe G, Sanders JE, Schmetzer H, Schmetzer H, Schmetzer HM, Schmid C, Seabright M, Seber A, Slovak ML, Sole F, Sole F, Thomas Duell, Tichelli A, Tichelli A, van Esser JW, Xu J, Yan J, Yoshida A   +46 more
core   +1 more source

Hemophagocytic Lymphohistiocytosis as First Manifestation of Dual B-Cell Neoplasms: A Case Report of Co-Existing Multiple Myeloma and B-Cell Lymphoma. [PDF]

EJHaem
ABSTRACT Hemophagocytic lymphohistiocytosis (HLH) is an immune disorder causing excessive inflammation and tissue damage. Lymphoma, especially T‐cell lymphoma, is the most common cause of HLH, while Multiple Myeloma (MM) is rarely associated. We present a 61‐year‐old man with spiking fevers, fatigue, and unintentional weight loss. The HLH was driven by
Romagnoli C, Lyubimova A, Santos-Carrion L, Alloush F, Sriganeshan V, Noboa A, Barrientos JC.   +6 more
europepmc   +2 more sources

A rare cause of pancytopenia: Sheehan′s syndrome

Medical Journal of Dr. D.Y. Patil University, 2015
Sheehan′s syndrome is characterized by varying degrees of anterior pituitary dysfunction due to postpartum ischemic necrosis of the pituitary gland after massive bleeding. Pancytopenia is rarely observed in patients with Sheehan′s syndrome.
Mustafa Volkan Demir, Selçuk Yaylaci, Tuba Öztürk Demir, Tayfun Temiz, Ahmet Bilal Genç   +4 more
doaj   +1 more source

A Rare Cause of Drug-Induced Pancytopenia: Trimethoprim–Sulfamethoxazole-Induced Pancytopenia

Clinics and Practice, 2021
Pancytopenia is a decrease across cellular hematological lines. Many different etiologies can cause this clinical picture including viral and bacterial infections, chemicals, malignancy, and medications.
Khalid Sawalha, Philip T. Sobash, Gilbert-Roy Kamoga   +2 more
doaj   +1 more source

Digenic Functional B12 and Folate Defect Mimicking Myelodysplasia. [PDF]

Clin Case Rep
Proposed mechanistic model of mutation‐related outcomes. ABSTRACT A digenic defect involving CUBN and MTHFR produced functional B12/folate deficiency in a patient with pancytopenia and neurological signs, mimicking myelodysplasia. Genetic and metabolic screening revealed elevated methylmalonic acid/homocysteine, with rapid remission post‐parenteral B12.
Cluzeau T, Oussalah A, Silva Rodriguez M, Naïmi M.   +3 more
europepmc   +2 more sources