Purpura
, Ecchymosis, Thrombocytopenia
These
conditions can be misdiagnosed as SBS, or supporting symptoms of "abuse"
"Systemic
reactions from
vaccines include fever, irritability,
loss of appetite, sleepiness and
inconsolable crying. (22)
Vaccines have also been shown to possibly produce more concerning
symptoms such as purpura, ecchymosis, thrombocytopenia
(23),
and other conditions that cause brain
swelling (43,
44, 45, 46) or increased intracranial pressure
(47, 48, 49) in
a recognized percentage of children.(50)" |
dictionary.com
:
Purpura--any of several hemorrhagic states characterized
by patches of purplish discoloration resulting from extravasation
of blood into the skin and mucous membranes —see THROMBOCYTOPENIC
PURPURA
Ecchymosis--1.
the purple or black-and-blue area resulting from a bruise
2. the escape of blood from ruptured blood vessels into the surrounding
tissue to form a purple or black-and-blue
spot on the skin
Thrombocytopenia--persistent
decrease in the number of blood platelets that is often associated
with hemorrhagic conditions called also thrombopenia —throm·bo·cy·to·pe·nic
/-nik/ adjective
http://www.medicaljournal-ias.org/15_4/Sakha.pdf
HEPATITIS B VACCINATION AND INFANTILE IDIOPATHIC
THROMBOCYTOPENIC PURPURA
KAZEM SAKHA*
ARMAN MALEKIAN*
SAID ASLANABADI*
SUMMARY: Since 1993, Iranian infants
have been routinely vaccinated against hepatitis B. In the period
of 1993-2002, twenty five children with infantile thrombocytopenic
purpura (ITP) were admitted to the Childrens Medical Center
in Tabriz, Iran whereas between 1982 and 1992, only two cases were
hospitalized with the same diagnosis. This suggests a cause and effect
relationship between hepatitis B vaccination and ITP.
INTRODUCTION
ITP is an autoimmune disorder leading to a reduction of the number
of peripheral blood platelets (1). For reasons not well understood,
autoantibodies are generated against glycoproteins GpIb/Ix and GpIIb/IIIa
and are stiuated on the surface of the platelets. Attachment of autoantibodies
to these surface antigens leads to phagocytosis or
complement-induced lysis of the platelets involved. This process may
also involve megakaryocytes, leading to a decrease in platelet production
(2,4). Autoantibodies against platelet surface antigens have been
detected in 75% of the patients (2,3).
ITP appears in two forms: acute or chronic. The acute form occurs
predominantly in children. 85% of cases are preceded by a viral infection.
The disorder may last for one or two months period and is self limited.
Mumps, measles, rubella vaccine (MMR) has been implicated in the etiology
of ITP (5-10). In Finland, 23 cases of ITP were reported among 70.000
MMR vaccines. The authors speculated that the vaccine leads to generation
of antiplatelet antibodies (1). In another study, one case of ITP
was recorded among 24.000 MMR vaccines (10).
Occurrence of ITP following DPT vaccination is rare. In a British
study, only two cases were reported (8), this data is not significant
when the widespread administration of
DPT vaccine is considered. Two cases of ITP have been reported in
conjunction with small pox vaccination (12). Small numbers of cases
following recombinant HBV have
been reported (13). There is no report of ITP following plasma-derived
hepatitis vaccine (11).
MATERIALS AND METHODS
ITP cases between 1992 and 2002
The files of all 25 infants under six months of age, hospitalized
at the Childrens Medical Center in Tabriz, Iran, between 1993 and
2002 and discharged with ITP as the final diagnosis were included
in the present study. The diagnosis was established based on the clinical
findings (purpura, ecchymosis), platelet count, bone marrow findings
and exclusion of other causes.
*From Department of Pediatrics, Tabriz University of Medical
Sciences, Tabriz, Iran.
Medical Journal of Islamic World Academy of Sciences 15:4, 149-151,
2005
http://adc.bmj.com/cgi/content/abstract/84/3/227
Article
Short report
Idiopathic thrombocytopenic
purpura and MMR vaccine E Millera, P Waighta, C P Farringtonb, N Andrewsa,
J Stowec, B Taylorc
a Immunisation Division,
Public Health Laboratory Service Communicable Disease Surveillance
Centre, Colindale, London NW9 5EQ, UK, b Department of Statistics,
The Open University, Milton Keynes MK7 6AA, UK, c Royal Free Campus,
Royal Free and University College Medical School, University College
London, London NW3 2PF, UK
Correspondence to: Dr Miller
e.miller@phls.co.uk
Accepted 11 April 2000
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=PubMed&list_uids=12534647&dopt=AbstractPlus
A CAUSAL ASSOCIATION BETWEEN MEASLES---mumps-rubella (MMR) vaccine
and idiopathic thrombocytopenic purpura (ITP) was confirmed using
immunisation/hospital admission record linkage. The absolute risk
within six weeks of immunisation was 1 in 22 300 doses, with two of
every three cases occurring in the six week post-immunisation period
being caused by MMR.
1: Br J Clin Pharmacol.
2003 Jan;55(1):107-11.
MMR vaccine and idiopathic thrombocytopaenic purpura.
Black C, Kaye JA, Jick H.
Department of Public Health,
Aberdeen University, Aberdeen, UK. corri.black@abdn.ac.uk
AIMS: To estimate the
relationship between idiopathic thrombocytopaenic purpura (ITP) and
the measles, mumps and rubella (MMR) vaccination in children; calculating
the relative risk estimate for ITP with in 6 weeks after MMR vaccination
and the attributable risk of ITP within 6 weeks after MMR vaccination.
METHODS: Using the General Practice Research Database we identified
children with a first-time diagnosis of ITP from a base population
of children aged less than 6 years between January 1988 and December
1999. After describing the characteristics of all the children identified
with ITP, we focused on cases aged 13-24 months to perform a population-based,
case-control analysis to estimate the relative risk of developing
ITP within 6 weeks after MMR vaccination. We also calculated the risk
of ITP attributable to the MMR vaccination. RESULTS: Sixty-three children
with a first time diagnosis of ITP were identified; 23 cases were
between 13 and 24 months old. The relative risk estimate for ITP within
6 weeks after MMR vaccination, compared to the combined group of unvaccinated
children and children vaccinated with MMR more than 26 weeks previously
was 6.3 (95% CI 1.3-30.1). The attributable risk of developing ITP
within 6 weeks after MMR vaccination was estimated to be 1 in 25,000
vaccinations (95% confidence interval 21,300, 89,400). CONCLUSION:
This study confirms the increased risk of ITP within 6 weeks after
MMR vaccination. However, the attributable risk of ITP within 6 weeks
after MMR vaccination is low.
PMID: 12534647 [PubMed
- indexed for MEDLINE]
http://www.ingentaconnect.com/content/mksg/ejh/2006/00000077/00000004/art00010
Acute immune thrombocytopenic purpura in infants: associated
factors, clinical features, treatment and long-term outcome
Authors: Wang, Jiaan-Der; Huang, Fang-Liang1; Chen, Po-Yen2;
Wang, Teh-Ming3; Chi, Ching-Shiang1; Chang, Te-Kau1
Source: European Journal of Haematology, Volume 77, Number
4, October 2006 , pp. 334-337(4)
Abstract:
Wang J-D, Huang F-L, Chen P-Y, Wang T-M, Chi C-S, Chang T-K. Acute
immune thrombocytopenic purpura in infants: associated factors, clinical
features, treatment and long-term outcome.
The natural course of acute
immune thrombocytopenic purpura (ITP) in infants is poorly described
in the literature. A retrospective study of 17 consecutive patients
<1?yr of age admitted and treated for acute ITP between 1996 and
2005 was conducted. We investigated their demographics, vaccination
history, clinical features, laboratory examinations, response to treatment
and long-term outcome. There were 11 male and six female infants.
Their ages ranged from 24?d to 12?months with a median of 3?months.
All infants presented with petechiae
and/or ecchymoses. Fourteen cases had platelet counts
below 20?×?109/L at the time of admission. They all had good
response to a single course of treatment (14/17) or multiple courses
of treatment (3/17). None had progressed into chronic ITP. Seven
infants had a causal relationship with immunization,
five associated with hepatitis B,
one diphtheria-pertussis-tetanus,
one diphtheria-tetanus-acellular pertussis-inactivated
poliovirus vaccine-conjugated Haemophilus influenza vaccines.
These seven infants responded to treatment within 3-9?d after therapy
with intravenous immunoglobulin, high-dose methylprednisolone or oral
steroids. Re-boosters with vaccines revealed no recurrence of the
disease in all of these seven patients. The study suggests that further
immunization is not contraindicated in infants experiencing acute
ITP associated with vaccines.
http://www.chiro.org/LINKS/ABSTRACTS/Issues_in_Chiropractic_Pediatrics.shtml
Thrombocytopenia:
vaccinations, drugs, or disease-caused
Abnormal bleeding, bruising, subdural hematomas,
retinal hemorrhages
(symptoms falsely attributed exclusively to
Shaken Baby Syndrome)
" Generally speaking,
in humans, a normal platelet count ranges from 150,000 and 450,000
per mm3 (microlitre).[1] These limits, however, are determined by
the 2.5th lower and upper percentile, and a deviation does not necessarily
imply any form of disease. The number of platelets in a blood sample
also decreases rather quickly with time and a low platelet count may
be caused by a delay between sampling and analysis." --Wikipedia
Photos of a condition
associated with vaccinations, drugs, and original disease from unknown
causes, resulting in abnormal bruising, hemorrhagic conditions, retinal
hemorrhage, subdural hematoma, bleeding in the brain (symptoms associated
with SBS cases, whose "experts" falsely claim are exclusive
to "shaken babies")
Online
pictures of thrombocytopenia
from different medical websites
|
|
Thrombocytopenia:
Retinal Hemorrhages
Photos of a condition associated
with vaccinations, drugs, and original disease from unknown causes,
resulting in abnormal bruising,
hemorrhagic conditions, retinal hemorrhage, subdural hematoma, bleeding
in the brain

Types of retinal hemorrhages

http://www.google.com/search?q=thrombocytopenia+%2B+retinal+hemorrhage
(37,100 hits)
Massive
bilateral vitreoretinal hemorrhage in patient with chronic ...
thrombocytopenia [4]. The retinal hemorrhages were generally flame-shaped,
but were occasionally
either subhyaloid or had broken through the internal ...
www.springerlink.com/index/WU362673512801QW.pdf
Vaccine-induced THROMBOCYTOPENIA journal
articles (a small sample from http://scholar.google.com)
- THROMBOCYTOPENIA
AFTER IMMUNIZATION WITH MEASLES VACCINES:
REVIEW OF THE VACCINE ADVERSE EVENTS REPORTING SYSTEM (1990 TO
1994). Brief Report
Pediatric Infectious Disease Journal. 15(1):88-90, January 1996.
Beeler, Judy M.D.; Varricchio, Frederick M.D.; Wise, Robert M.D.,
M.P.H.
- An
overview of the vaccine adverse event reporting system (VAERS)
as a surveillance system - all 4 versions »
JA Singleton, JC Lloyd, GT Mootrey, ME Salive, RT … - Vaccine,
1999 - Elsevier
... Update: vaccine side effects, adverse reactions, contraindications
... and R. Wise,
Thrombocytopenia after immunization with ... of the vaccine adverse
events reporting ...
- Postmarketing
Surveillance and Adverse Drug Reactions Current Perspectives and
Future Needs - all 4 versions »
T Brewer, GA Colditz - JAMA, 1999 - Am Med Assoc
... vaccination and febrile convulsions or idiopathic thrombocytopenia
purpura after ...
data have been used to describe previously unreported vaccine
adverse effects. ...
- Clin
Exp Rheumatol. 2004 Nov-Dec;22(6):749-55.Links
A case-series of adverse events, positive re-challenge of symptoms,
and events in identical twins
following hepatitis B vaccination: analysis of the Vaccine Adverse
Event Reporting System
(VAERS) database and literature review.
Geier MR, Geier DA.
The Genetic Centers of America, MedCon, Inc., Silver Spring, Maryland
20905, USA. mgeier@comcast.net
-
OBJECTIVES: Adverse events and positive re-challenge of symptoms
reported in the scientific literature and to the Vaccine Adverse
Event Reporting System (VAERS) following hepatitis B vaccination
(HBV) were examined. METHODS: The VAERS and PubMed (1966-2003)
were searched for autoimmune conditions including arthritis, rheumatoid
arthritis, myelitis, optic neuritis, multiple sclerosis (MS),
Guillain Barré Syndrome (GBS), glomerulonephritis, pancytopenia/thrombocytopenia,
fatigue, and chronic fatigue, and Systemic Lupus Erythematous
(SLE) following HBV. RESULTS: HBV was associated with a number
of serious conditions and positive re-challenge or significant
exacerbation of symptoms following immunization. There were 415
arthritis, 166 rheumatoid arthritis, 130 myelitis, 4 SLE, 100
optic neuritis, 101 GBS, 29 glomerulonephritis, 283 pancytopenia/thrombocytopenia,
and 183 MS events reportedfollowing HBV A total of 465 positive
re-challenge adverse events were observed following adult HBV
that occurred sooner and with more severity than initial adverse
event reports. A case-report of arthritis occurring in identical
twins was also identified. CONCLUSIONS: Evidence from biological
plausibility, case-reports, case-series, epidemiological, and
now for positive re-challenge and exacerbation of symptoms, and
events in identical twins was presented. One would have to consider
that there is causal relationship between HBV and serious autoimmune
disorders among certain susceptible vaccine recipients in a defined
temporal period following immunization. In immunizing adults,
the patient, with the help of their physician, should make an
informed consent decision as to whether to be immunized or not,
weighing the small risks of the adverse effects of HBV with the
risk of exposure to deadly hepatitis B virus.
-
1:
N Y State J Med. 1972 Feb 15;72(4):499.Links
Thrombocytopenia associated with rubella vaccination.
Bartos HR.
-
The
Ricochet of Magic Bullets: Summary of the Institute of Medicine
Report, Adverse Effects of Pertussis and Rubella Vaccines
Christopher P. Howson PhD1 and Harvey V. Fineberg MD, PhD1
1
From the Institute of Medicine of the National Academy of Sciences,
Washington, DC. Dr Howson is Deputy Director of the Division of
International Health of the Institute of Medicine and Dr Fineberg
is dean of the Harvard School of Public Health, Boston, MA.
On
July 3, 1991, the National Academy of Sciences' Institute of Medicine
(IOM) released a reported entitled, Adverse Effects of Pertussis
and Rubella Vaccines,1 in response to a congressional request
to review evidence about a set of serious adverse events and immunization
with pertussis and rubella vaccines. The request originated in
the 1986 National Childhood Vaccine Injury Act (Public Law 99-660),
whose primary purpose was to establish a federal compensation
scheme for persons potentially injured by a vaccine; Section 312
of Public Law 99-660 called for the IOM review.
Over
the course of its 20-month study, the 11-member interdisciplinary
committee constituted by IOM to conduct the review examined altogether
18 adverse events for pertussis vaccine—infantile spasms;
hypsarhythmia; aseptic meningitis; acute encephalopathy; chronic
neurologic (permanent brain) damage; deaths classified as sudden
infant death syndrome (SIDS); anaphylaxis, autism; erythema multiforme
or other rashes; Guillain-Barré syndrome (polyneuropathy);
peripheral mononeuropathy; hemolytic anemia; juvenile diabetes;
learning disabilities and hyperactivity; protracted inconsolable
crying or screaming; Reye's syndrome; shock and "unusual
shock-like state" with hypotonicity, hyporesponsiveness,
and short-lived convulsions (usually febrile); and thrombocytopenia—and
4 adverse events for rubella vaccine—acute arthritis; chronic
arthritis; radiculoneuritis and other neuropathies; and thrombocytopenic
purpura. In conducting its review, the committee recognized that
its charge was to focus on questions of causation and not broader
topics, such as cost-benefit or risk-benefit analyses of vaccination.
This
summary begins with a brief history of events leading to the IOM
study, then reviews the methods used by the committee to evaluate
the evidence, summarizes the committee's conclusions for these
adverse events, and offers directions for future investigation
of adverse events in connection with widely used health interventions,
such as vaccination.
Submitted on November 5, 1991
Accepted on November 21, 1991
-
Hepatitis
and death following vaccination with 17D-204 yellow fever
vaccine - all 3 versions »
RC Chan, DJ Penney, D Little, IW Carter, JA … - The Lancet,
2001 - Elsevier
... to by: Rarity of adverse effects after 17D ... on Jan 31,
he developed thrombocytopenia,
clotting abnormalities ... not support previous yellow fever vaccination
in our ...
-
Comment
on:
Lancet. 1994 Nov 5;344(8932):1293.
Thrombocytopenia
reported in association with hepatitis B and A vaccines.
Meyboom RH, Fucik H, Edwards IR.
http://tinyurl.com/4z2za8


Drug-Induced
THROMBOCYTOPENIA
http://www.neurology.org/cgi/content/abstract/54/6/1240
Neurologic complications
in immune-mediated heparin-induced thrombocytopenia
C. Pohl, MD, U. Harbrecht, MD, A. Greinacher, MD, I. Theuerkauf, MD,
R. Biniek, MD, P. Hanfland, MD and T. Klockgether, MD
From the Departments of
Neurology (Drs. Pohl and Klockgether), Transfusion Medicine (Drs.
Pohl, Harbrecht, and Hanfland) and Pathology (Dr. Theuerkauf), Rheinische
Friedrich Wilhelms Universität, Bonn; Institute of Immunology
and Transfusion Medicine (Dr. Greinacher), Ernst Moritz Arndt Universität
Greifswald; and the Rheinische Landesklinik Bonn (Dr. Biniek), Bonn,
Germany.
Address correspondence
and reprint requests to Dr. C. Pohl, Department of Neurology, University
of Bonn, Sigmund-Freud-Straße, D-53105 Bonn, Germany; e-mail:
c.pohl@uni-Bonn.de
OBJECTIVE: To evaluate
neurologic complications in patients with immune-mediated heparin-induced
thrombocytopenia (HIT) with respect to incidence, clinical characteristics,
outcome, and therapy.
METHODS: One hundred and
twenty consecutive patients with immune-mediated HIT were recruited
over a period of 11 years and studied retrospectively for the occurrence
of neurologic complications. Diagnosis of HIT was based on established
clinical criteria and confirmed by detection of heparin-induced antibodies
using functional and immunologic tests.
RESULTS: Eleven of the
120 patients (9.2%) presented with neurologic complications; 7 suffered
from ischemic cerebrovascular events, 3 from cerebral venous thrombosis,
and 1 had a transient confusional state during high-dose heparin administration.
Primary intracerebral hemorrhage was not observed. The relative mortality
was much higher (Chi-square test, p < 0.01) in HIT patients with
neurologic complications (55%) as compared to patients without neurologic
complications (11%). The mean platelet count nadir in neurologic patients
was 38 ± 25 x 109/l on average, and was lower in patients with
fatal outcome compared to those who survived (21 ± 13 x 109/l
versus 58 ± 21 x 109/l; p < 0.05, Wilcoxon test). In three
patients neurologic complications preceded thrombocytopenia. There
was a high coincidence of HIT-associated neurologic complications
with other HIT-associated arterial or venous thrombotic manifestations.
CONCLUSION: Neurologic
complications in HIT are relatively rare, but associated with a high
comorbidity and mortality. HIT-associated neurologic complications
include cerebrovascular ischemia and cerebral venous thrombosis. They
may occur at a normal platelet count











http://medicineworld.org/physicians/hematology/thrombocytopenia.html

Figure 2. Computed tomography demonstrating large right frontal intracerebral
hemorrhage.
