Microangiopathic hemolytic anemia differential diagnosis: Difference between revisions

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{{Microangiopathic hemolytic anemia}}  
{{Microangiopathic hemolytic anemia}} {{AE}} {{MSJ}}
 
 
[[Microangiopathic hemolytic anemia]] must be differentiated from following [[disease]]s<ref name="pmid29875054">{{cite journal| author=Bommer M, Wölfle-Guter M, Bohl S, Kuchenbauer F| title=The Differential Diagnosis and Treatment of Thrombotic Microangiopathies. | journal=Dtsch Arztebl Int | year= 2018 | volume= 115 | issue= 19 | pages= 327-334 | pmid=29875054 | doi=10.3238/arztebl.2018.0327 | pmc=5997890 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=29875054  }} </ref>:
{| style="border: 0px; font-size: 90%; margin: 3px;" align=center
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! style="background: #4479BA; width: 120px;" | {{fontcolor|#FFF|Disease}}
! style="background: #4479BA; width: 550px;" | {{fontcolor|#FFF|Findings}}
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| style="padding: 5px 5px; background: #DCDCDC;" | '''Pseudo-TTP ([[Vitamin B12]] deficiency)'''
| style="padding: 5px 5px; background: #F5F5F5;" |
* [[Patient]]s have [[neurological]] symptoms like [[numbness]], [[ataxic]] gait and [[tingling]] along with [[macrocytic anemia]].
* There is a reduced level of [[reticulocyte]]s, with elevated levels of [[LDH|Lactate dehydrogenase]] (i.e. greater than 5000 U/L), methylmalonate, and homocysteine.
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| style="padding: 5px 5px; background: #DCDCDC;" | '''[[Pregnancy]] induced [[fatty liver]]'''
| style="padding: 5px 5px; background: #F5F5F5;" |
* [[Patient]]s presents with [[right upper quadrant]] or [[epigastric]] [[abdominal pain]], [[nausea]] and [[vomiting]].
* On laboratory work-up, there is [[hypoglycemia]] along with deranged [[liver function tests]].
 
* There is elevated levels of [[bilirubin]], [[alanine aminotransferase]], [[aspartate aminotransferase]], reduced [[antithrombin III]] and [[coagulation factor]]s level<ref name="pmid16432556">{{cite journal| author=Ko H, Yoshida EM| title=Acute fatty liver of pregnancy. | journal=Can J Gastroenterol | year= 2006 | volume= 20 | issue= 1 | pages= 25-30 | pmid=16432556 | doi=10.1155/2006/638131 | pmc=2538964 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16432556  }} </ref>.
|-
| style="padding: 5px 5px; background: #DCDCDC;" | '''[[DIC|Disseminated intravascular coagulation]]'''
| style="padding: 5px 5px; background: #F5F5F5;" |
* Can occur in [[sepsis]], and different malignancies like [[prostate cancer]], [[Acute promyelocytic leukemia]] and [[Gastric cancer]], there in increased consumption of [[fibrin]].
* On laboratory work-up, there is reduced [[fibrinogen]] level, [[Auer rod]] in [[Acute promyelocytic leukemia]] and leukoerythroblastic picture, with nucleated [[red blood cell]s, [[poikilocytosis]], left shift of [[white blood cells]].
* In [[sepsis]], there is elevation of [[procalcitonin]] along with positive [[blood culture]] and reduced levels of [[coagulation factors]]. 
|-
| style="padding: 5px 5px; background: #DCDCDC;" |'''[[Endocarditis]]'''
| style="padding: 5px 5px; background: #F5F5F5;" |
* [[Patient]]s have multi-system involvement presenting with [[fever]], [[sepsis]], poly[[artharalgia]], [[Janeway lesion]], [[Osler’s node]], and a new-onset or changed [[heart]] [[murmur]]. 
* It is diagnosed clinically by Duke’s criteria.
* It is confirmed by [[blood]] [[culture]] and trans-esophageal [[echocardiography]].
|-
| style="padding: 5px 5px; background: #DCDCDC;" | '''[[Evan's syndrome]]'''
| style="padding: 5px 5px; background: #F5F5F5;" |
* [[Immune]] mediated [[thrombocytopenia]] and [[autoimmune hemolytic anemia]].
* [[Coombs test]] positive. On [[peripheral blood smear]], there are no [[schistocytes]].
|-
| style="padding: 5px 5px; background: #DCDCDC;" | '''[[Antiphospholipid syndrome]]'''
| style="padding: 5px 5px; background: #F5F5F5;" |
* Women have a history of [[arterial|artery]] thrombi and [[deep venous thrombosis]] in lower extremeties, recurrent [[abortion]], [[stroke]] and headache.
* These patients have prolonged activated [[partial thromboplastin time]] and positive serology for [[anti-cardiolipin antibodies]].
|-
| style="padding: 5px 5px; background: #DCDCDC;" | '''[[Malaria]], [[Babesiosis]]'''
| style="padding: 5px 5px; background: #F5F5F5;" |
* [[Patient]]s presents with periodic spikes of high-grade [[fever]] with [[rigor]]s, [[chill]]s, [[nausea]], [[vomiting]], [[fatigue]], [[myalgia]] and malaise.
* The intra-[[cell]]ular [[parasite]] are identified on special stained [[peripheral blood smear]].
|-
| style="padding: 5px 5px; background: #DCDCDC;" | '''[[Viral]] [[Infection]]s'''
| style="padding: 5px 5px; background: #F5F5F5;" |
* In specific [[viral]] [[disease]]s like [[Dengue]] hemorrhagic fever, [[hantavirus]] and [[filoviridae]], there is significant [[thrombocytopenia]].
* [[Patient]]s have a recent history of travel.
* There are no signs of [[hemolysis]] on laboratory workup.
|}
 


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==References==
==References==
{{Reflist|2}}
{{Reflist|2}}

Latest revision as of 20:59, 28 January 2021

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Microangiopathic hemolytic anemia must be differentiated from following diseases[1]:

Disease Findings
Pseudo-TTP (Vitamin B12 deficiency)
Pregnancy induced fatty liver
Disseminated intravascular coagulation
Endocarditis
Evan's syndrome
Antiphospholipid syndrome
Malaria, Babesiosis
Viral Infections


References

  1. Bommer M, Wölfle-Guter M, Bohl S, Kuchenbauer F (2018). "The Differential Diagnosis and Treatment of Thrombotic Microangiopathies". Dtsch Arztebl Int. 115 (19): 327–334. doi:10.3238/arztebl.2018.0327. PMC 5997890. PMID 29875054.
  2. Ko H, Yoshida EM (2006). "Acute fatty liver of pregnancy". Can J Gastroenterol. 20 (1): 25–30. doi:10.1155/2006/638131. PMC 2538964. PMID 16432556.

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