keyword
MENU ▼
Read by QxMD icon Read
search

megaloblastosis

keyword
https://www.readbyqxmd.com/read/26861098/-maternal-crohn-s-disease-related-vitamin-b12-deficient-megaloblastic-anemia-in-an-infant
#1
REVIEW
Wataru Ohyama, Masayoshi Yamaoka, Kentaro Yokoi, Megumi Iwahashi, Yuka Inage, Seiji Arihiro, Kazutaka Koganei, Akira Sugita, Hiroyuki Ida, Masaharu Akiyama
We report an 11-month-old breast-fed boy with feeding difficulties, lethargy, and developmental delay. Blood examination showed pancytopenia and decreased serum levels of vitamin B12. Anisocytosis and poikilocytes were detected in his peripheral blood, and increased megaloblastosis without leukemic cells was detected in his bone marrow. After the diagnosis of megaloblastic anemia due to vitamin B12 deficiency, symptoms were improved by vitamin B12 administration. Further investigation of the mother identified Crohn's disease and suggested that the supply of vitamin B12 from the mother to the infant, via the placenta during pregnancy and via breast milk after birth, was decreased due to impaired absorption of vitamin B12 in the mother's small intestine...
January 2016: [Rinshō Ketsueki] the Japanese Journal of Clinical Hematology
https://www.readbyqxmd.com/read/25068715/early-markers-of-occult-megaloblastosis-for-low-cost-detection-of-hyperhomocysteinemia-in-patients-with-ischaemic-stroke-preventive-approach-for-primary-health-care
#2
Sohini Sengupta Neogi, Monica Thomas, Archna Sharma, Jaishree Kumar, Uma Khanduri
Recent studies have focussed on the association between elevated homocysteine levels with megaloblastic changes and thromboembolic events, but the relationship between occult megaloblastosis (with normal haemoglobin levels) and ischaemic stroke has not been widely explored. The objective of this study is to establish a simple and economical marker for the detection of occult megaloblastosis at the community health care level in developing countries. A hundred patients who met the inclusion criteria were studied...
September 2014: Canadian Journal of Physiology and Pharmacology
https://www.readbyqxmd.com/read/24490639/an-outbreak-of-pyrimethamine-toxicity-in-patients-with-ischaemic-heart-disease-in-pakistan
#3
Muhammad Zaman Khan Assir, Hafiz Ijaz Ahmad, Javed Akram, Noshin Wasim Yusuf, Umair Kamran
We investigated an outbreak of darkening of skin, bleeding from multiple sites, leucopenia and thrombocytopenia in ischaemic heart disease patients. Case patients were defined as patients who had received medicines from the pharmacy of Punjab Institute of Cardiology between 1 December 2011 and 12 January 2012 and who developed any one of the following: darkening of skin, bleeding from any site, thrombocytopenia and leucopenia. Clinical and drug-related data were abstracted. All 664 case patients had received iso-sorbide-mono-nitrate contaminated with about 50 mg of pyrimethamine, and 151 (23%) died...
September 2014: Basic & Clinical Pharmacology & Toxicology
https://www.readbyqxmd.com/read/24238033/an-etiological-reappraisal-of-pancytopenia-largest-series-reported-to-date-from-a-single-tertiary-care-teaching-hospital
#4
Arvind Jain, Manjiri Naniwadekar
BACKGROUND: Peripheral pancytopenia is not a disease by itself; rather it describes simultaneous presence of anemia, leucopenia and thrombocytopenia resulting from a number of disease processes. Only a few systematic studies have been published on the topic of pancytopenia, although extensive studies have been done for its different etiological factors like aplastic anemia, megaloblastic anemia, leukemia, etc. Thus, this study was carried out to investigate for and to identify the causes of pancytopenia, to find out the frequency of different causes, to determine the incidence of pancytopenia in relation to sex and age and to compare our findings with those of other similar studies from this part of the world...
2013: BMC Hematology
https://www.readbyqxmd.com/read/23343210/human-parvovirus-b19-infection-in-a-renal-transplant-recipient-a-case-report
#5
Michelle Teodoro Alves, Sandra Simone Vilaça, Maria das Graças Carvalho, Ana Paula Fernandes, Luci Maria Sant' Ana Dusse, Karina Braga Gomes
BACKGROUND: Parvovirus B19 presents tropism for human erythroid progenitor cells, causing chronic anemia in organ transplant recipients, due to their suppressed humoral and cellular responses. Diagnosis may be achieved through serological tests for detection of anti-B19 antibodies. However, renal transplant recipients are not routinely tested for parvovirus B19 infection, since there is scanty data or consensus on screening for B19 infection, as well as for treatment or preventive management of transplanted patients...
2013: BMC Research Notes
https://www.readbyqxmd.com/read/22764443/-etiological-profile-of-pancytopenia-in-adults-in-marrakesh-morocco
#6
H Nafil, I Tazi, M Sifsalam, M Bouchtia, L Mahmal
This retrospective study evaluated the frequency of different causes of pancytopenia in all adult patients with pancytopenia presenting to the Department of Haematology of Mohamed VI Hospital, Marrakesh from 1 January 2008 to 31 December 2010. A total of 118 cases of pancytopenia were found (average of 39 cases per year). The mean age of patients was 52 years (range 18-82 years) and 52.5% were male. The main clinical signs were pallor (100%), asthenia (100%) and fever (30.5%). Mean haemoglobin was 6.5 g/dL (range 2...
May 2012: Eastern Mediterranean Health Journal, la Revue de Santé de la Méditerranée Orientale
https://www.readbyqxmd.com/read/22338992/mast-cell-activation-syndrome-masquerading-as-agranulocytosis
#7
Lawrence B Afrin
Acquired agranulocytosis is a rare, life-threatening disorder. The few known causes/associations usually are readily identifiable (e.g., drug reaction, Felty syndrome, megaloblastosis, large granular lymphocytic leukemia, etc.). We report a novel association with mast cell disease. A 61-year-old morbidly obese man developed rheumatoid arthritis unresponsive to several medications. Agranulocytosis developed shortly after sulfasalazine was started but did not improve when the drug was soon stopped. Other symptoms across many systems developed including hives and presyncope...
January 2012: Military Medicine
https://www.readbyqxmd.com/read/21279100/the-etiology-and-management-of-leukopenia
#8
V W Ing
Leukopenia is an abnormal reduction of circulating white blood cells, especially the granulocytes. The term leukopenia is often used interchangeably with neutropenia. It may result from reduced production of white blood cells or increased utilization and destruction, or both. Infection, drugs, malignancy, megaloblastosis, hypersplenism and immunoneutropenia are responsible for most cases of neutropenia. Primary neutropenia is very rare. Sometimes, particularly in children, primary neutropenia is hereditary and may be associated with other developmental defects...
September 1984: Canadian Family Physician Médecin de Famille Canadien
https://www.readbyqxmd.com/read/21267137/serum-vitamin-b-12-and-folate-levels-in-women-taking-oral-contraceptives
#9
J A Mountifield
Serum vitamin B(12) and erythrocyte folate levels were determined in a group of healthy women eating a balanced diet. Approximately 50% were using oral contraceptives. Vitamin B(12) levels were lower in the oral contraceptive users. However, their folate levels were no different from those of non-users. Age had no effect on either vitamin B(12) or folate levels. Oral contraceptive users taking multiple vitamin tablets containing vitamin B(12) and folate had slightly higher folate levels, but their vitamin B(12) levels were no different from those of OC users who were not taking vitamin tablets...
April 1986: Canadian Family Physician Médecin de Famille Canadien
https://www.readbyqxmd.com/read/20206879/functional-vitamin-b12-deficiency-in-alcoholics-an-intriguing-finding-in-a-retrospective-study-of-megaloblastic-anemic-patients
#10
Alberto Fragasso, Clara Mannarella, Angela Ciancio, Andrea Sacco
BACKGROUND: Measurement of serum cobalamin levels is the standard investigation for assessing Vitamin B12 deficiency. However some patients with clinical evidence of cobalamin deficiency may have serum levels within the normal range. Since falsely increased values of cobalamin can be caused by alcoholic liver disease, we evaluated the impact of this disease on the diagnosis of cobalamin and folic acid deficiency. METHODS: We reviewed data of 101 adult patients with megaloblastic anemia assessed by measuring in parallel serum cobalamin, serum folate and red blood cell folate levels...
April 2010: European Journal of Internal Medicine
https://www.readbyqxmd.com/read/20148139/a-case-of-primary-biliary-cirrhosis-associated-with-pernicious-anemia-a-case-report
#11
Elhem Ben Jazia, Mabrouk Khalifa, Atef Ben Abdelkader, Naoufel Kaabia, Neirouz Ghannouchi, Ahlem Braham, Amel Letaief, Fethi Bahri
Primary biliary cirrhosis is often associated with autoimmune diseases. However, its association with pernicious anemia has rarely been reported.We report a case of a 68-year-old woman who presented jaundice and pruritus. Mildly elevated serum levels of alkaline phosphatase and gamma-glutamyl transpeptidase were detected. The titer of anti-mitochondrial M(2 )anti-body was elevated. Histology of liver biopsy showed features of primary biliary cirrhosis. In addition, aregenerative macrocytic anemia was found in the full blood count...
2010: Cases Journal
https://www.readbyqxmd.com/read/18136926/bone-marrow-changes-in-man-after-treatment-with-aminopterin-amethopterin-and-aminoanfol-with-special-reference-to-megaloblastosis-and-tumor-remission
#12
https://www.readbyqxmd.com/read/18136515/effects-of-4-amino-pteroylglutamic-acid-in-dogs-with-special-reference-to-megaloblastosis
#13
J B THIERSCH, F S PHILIPS
No abstract text is available yet for this article.
July 1949: Proceedings of the Society for Experimental Biology and Medicine
https://www.readbyqxmd.com/read/18085121/megaloblastic-anaemia-prevalence-and-causative-factors
#14
Uma Khanduri, Archna Sharma
BACKGROUND: Megaloblastic anaemia is not uncommon in India, but data are insufficient regarding its prevalence, and causative and precipitating factors. We did a prospective study to document such data for patients of megaloblastic anaemia. METHODS: All patients presenting to our hospital over a period of 6 months with a haemoglobin < 10 g/dl and/or mean corpuscular volume > 95 fL and blood film findings consistent with megaloblastosis were included in the study...
July 2007: National Medical Journal of India
https://www.readbyqxmd.com/read/17967337/life-threatening-megaloblastic-pancytopenia-with-normal-mean-cell-volume-case-series
#15
Jeevan Sekhar, Sally P Stabler
The mean red blood cell volume (MCV) is usually increased in severe megaloblastic anemia due to pernicious anemia. However, during one year in a university hospital, three patients with life-threatening pancytopenia and normal MCV were proven to have severe vitamin B12 deficiency. The red blood cell distribution width was markedly increased (three times normal) and led to review of the blood smear and recognition of megaloblastosis as well as prominent red cell fragmentation. These three cases illustrate that vitamin B12 status should be evaluated in cases of pancytopenia, independent of the MCV value...
November 2007: European Journal of Internal Medicine
https://www.readbyqxmd.com/read/16699466/the-utility-of-bone-marrow-examination-in-renal-transplantation-nine-years-of-experience-from-north-india
#16
Gurjeewan Garewal, Jasmina Ahluwalia, Vijay Kumar, Rajeev Shukla, Reena Das, Neelam Varma, Vinay Sakhuja
Renal transplantation may be complicated by persistent fever and cytopenia. Bone marrow examination, though painful and invasive, may be of value because it can be performed in most peripheral hospitals, and the results are rapidly available. In a retrospective analysis, clinical records, marrow aspirates, and trephine biopsies were assessed to determine the indications for bone marrow examination and the findings in 132 patients over a 9-year period. In 7 of 61 (11%) patients with fever, a specific infection or a malignancy was identified, and hypocellularity was seen in 85% of cases...
May 15, 2006: Transplantation
https://www.readbyqxmd.com/read/16540210/-neurological-manifestations-of-vitamin-b12-deficiency-a-retrospective-study-of-26-cases
#17
COMPARATIVE STUDY
M Maamar, Z Tazi-Mezalek, H Harmouche, W Ammouri, M Zahlane, M Adnaoui, M Aouni, A Mohattane, A Maaouni
PURPOSE: Neurological symptoms of B12 vitamin deficiency are polymorph. Causes are dominated by Biermer's disease and B12 vitamin non dissociation that is frequent in the elderly. METHODS: We realized a retrospective study during 11 years. Patients with neurological symptoms associated to megaloblastosis were included. Treatment with B12 vitamin lead to haematological manifestation regression. RESULTS: 26 cases were analyzed. Mean age was 50+/-14...
June 2006: La Revue de Médecine Interne
https://www.readbyqxmd.com/read/16252546/occult-cobalamin-and-folate-deficiency-in-indians
#18
Uma Khanduri, Archna Sharma, Arti Joshi
BACKGROUND: Our aim was to assess cobalamin and folate levels in normal Indian subjects before undertaking a prospective study of megaloblastic anaemia. METHODS: We took samples from 25 men and 25 women to establish the normal range. The exclusion criteria for subjects were age below 18 years and above 65 years, haemoglobin < 12 g/dl, and those who were pregnant, lactating or on any medication including vitamin supplements. A complete blood count and blood film examination for hypersegmented neutrophils were done...
July 2005: National Medical Journal of India
https://www.readbyqxmd.com/read/16103708/megaloblastosis-from-morphos-to-molecules
#19
K C Das, Monisha Das, D Mohanty, M M Jadaon, A Gupta, R Marouf, S K Easow
OBJECTIVE: Megaloblastosis (i.e., megaloblastic transformation of erythroid precursor cells in the bone marrow) is the cytomorphological hallmark of megaloblastic anemia resulting from vitamin B12 and folate deficiency. It is characterized by a finely stippled lacy pattern of nuclear chromatin, which is believed to be an expression of deranged cellular DNA synthesis. However, the molecular basis of these cytomorphological aberrations still remains obscure. The current presentation describes the results of our studies on some molecular events associated with the development of megaloblastosis...
2005: Medical Principles and Practice: International Journal of the Kuwait University, Health Science Centre
https://www.readbyqxmd.com/read/15607356/on-the-pathogenesis-of-erythroleukaemia-h0493
#20
REVIEW
T E Parry
In erythroleukaemia megaloblastic changes can co-exist with leukaemic changes in the marrow. The cause of the disease must therefore be such as can cause megaloblastosis and at the same time be mutagenic. Failure of the thymidylate synthelase reaction, the commonest cause of megaloblastic anaemia, can be eliminated in erythroleukaemia because (a) the dU suppression test is normal in the disease and (b) failure of the thymidylate synthelase reaction is not mutagenic. The deamination of both cytosine and adenine is mutagenic but the deamination of cytosine alone is apparent and the nucleotide of cytosine is the prime mutagenic nucleotide in leukaemia and cancer...
February 2005: Leukemia Research
keyword
keyword
114868
1
2
Fetch more papers »
Fetching more papers... Fetching...
Read by QxMD. Sign in or create an account to discover new knowledge that matter to you.
Remove bar
Read by QxMD icon Read
×

Search Tips

Use Boolean operators: AND/OR

diabetic AND foot
diabetes OR diabetic

Exclude a word using the 'minus' sign

Virchow -triad

Use Parentheses

water AND (cup OR glass)

Add an asterisk (*) at end of a word to include word stems

Neuro* will search for Neurology, Neuroscientist, Neurological, and so on

Use quotes to search for an exact phrase

"primary prevention of cancer"
(heart or cardiac or cardio*) AND arrest -"American Heart Association"