Victor W. T. Ling’s research while affiliated with National University Hospital - NUH and other places

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Publications (2)


Results of platelet count, anti-PF4 HIT ELISA and standard HIPA, and a summary of the treatment response.
Severe Thrombocytopenia, Thrombosis and Anti-PF4 Antibody after Pfizer-BioNTech COVID-19 mRNA Vaccine Booster—Is It Vaccine-Induced Immune Thrombotic Thrombocytopenia?
  • Article
  • Full-text available

November 2022

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68 Reads

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4 Citations

Victor W. T. Ling

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Bingwen Eugene Fan

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Soon Lee Lau

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Vaccine-induced immune thrombotic thrombocytopenia (VITT) is a serious and life-threatening complication occurring after adenovirus-vector COVID-19 vaccines, and is rarely reported after other vaccine types. Herein, we report a case of possible VITT after the Pfizer-BioNTech mRNA vaccine booster, who presented with extensive lower limb deep vein thrombosis, severe thrombocytopenia, markedly elevated D-dimer and positive anti-PF4 antibody occurring 2 weeks post-vaccination, concurrent with a lupus anticoagulant. A complete recovery was made after intravenous immunoglobulin, prednisolone and anticoagulation with the oral direct Xa inhibitor rivaroxaban. The presenting features of VITT may overlap with those of antiphospholipid syndrome associated with anti-PF4 and immune thrombocytopenia. We discuss the diagnostic considerations in VITT and highlight the challenges of performing VITT confirmatory assays in non-specialized settings. The set of five diagnostic criteria for VITT is a useful tool for guiding initial management, but may potentially include patients without VITT. The bleeding risks of severe thrombocytopenia in the face of thrombosis, requiring anticoagulant therapy, present a clinical challenge, but early recognition and management can potentially lead to favorable outcomes.

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An unusual presentation of Idiopathic hypereosinophilic syndrome

May 2020

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61 Reads

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6 Citations

Journal of Thrombosis and Thrombolysis

Hypereosinophilic syndrome (HES) is a rare but life-threatening multi-organ disease which can be complicated by stroke, with devastating outcomes. Eosinophils can accumulate in multiple organs, most commonly involving the heart, skin, lungs, spleen, and liver. Neurological end-organ complications in hypereosinophilic syndrome are unusual and have been established to be of three types: brain infarction, encephalopathy and sensory polyneuropathy. We present a case where acute ischaemic stroke and encephalopathy are early manifestations of Idiopathic HES. It is important to consider HES as an aetiology for stroke and a high eosinophil count is an initial diagnostic clue. Early initiation of steroid therapy can potentially prevent disease progression.

Citations (2)


... The condition is thought to be a class effect, but recent reports of its rare occurrence after the mRNA vaccine have emerged. 6 The diagnosis of VITT is not obvious and the differential diagnosis is crucial which includes essentially: COVID-19--associated coagulopathy, antiphospholipid syndrome (APS), thrombotic thrombocytopenic purpura (TTP), heparin-Induced thrombocytopenia (HIT) and immune thrombocytopenic purpura (ITP). 7 In our case, HIT and ITP are unlikely due to the absence of previous heparin exposure, and the presence of thrombotic events, respectively. ...

Reference:

A Rare Case of Vaccine-Induced Immune Thrombotic Thrombocytopenia After mRNA COVID Vaccine
Severe Thrombocytopenia, Thrombosis and Anti-PF4 Antibody after Pfizer-BioNTech COVID-19 mRNA Vaccine Booster—Is It Vaccine-Induced Immune Thrombotic Thrombocytopenia?

... 1 In some cases, HES is idiopathic, with no identifiable cause. 2 HES can present with acute or chronic symptoms affecting various organs and systems, including the brain, heart, lungs, liver, spleen, and bone marrow. 3,7 Neurological manifestations include ischemic stroke, venous sinus thrombosis, peripheral neuropathy, seizures, and encephalopathy. 3 Among these, HES-associated ischemic stroke is the most severe complication, occurring in 12% of patients with HES, with 10-15% of these cases affecting young adults. ...

An unusual presentation of Idiopathic hypereosinophilic syndrome
  • Citing Article
  • May 2020

Journal of Thrombosis and Thrombolysis