Related Experiment Video
Updated: May 24, 2026

07:49
Measuring Local Anaphylaxis in Mice
Published on: October 14, 2014
Anaphylaxis to Patent Blue V: a case series
Ania L Manson1, Rohit Juneja, Robert Self
1Department of Clinical Immunology, St Mary's Hospital, Imperial College Healthcare NHS Trust, London, W2 1NY, UK.
Asia Pacific Allergy
|February 21, 2012
Summary
Patent Blue V (PBV) dye used in sentinel lymph node biopsy (SLNB) can cause anaphylaxis. Early identification of PBV allergy is crucial for patient safety, especially with repeat procedures.
Area of Science:
- Medical Diagnostics
- Allergy Research
- Oncology Procedures
Background:
- Blue dyes like Patent Blue V (PBV) are standard in sentinel lymph node biopsy (SLNB) for breast cancer staging.
- Anaphylaxis is a known, potentially life-threatening risk associated with PBV dye exposure.
- The frequency of PBV allergy is estimated at 0.9%.
Observation:
- This study reports on four patients experiencing suspected anaphylaxis after SLNB.
- Clinical features, serum mast-cell tryptase (MCT), and skin prick test (SPT) results were analyzed.
- These tests are used to investigate Type-1 mediated hypersensitivity reactions.
Findings:
- The study details the clinical presentations and diagnostic test results for patients with suspected PBV-induced anaphylaxis.
- Analysis of MCT and SPT results in the context of clinical symptoms following PBV exposure.
- The findings underscore the importance of recognizing allergy following initial PBV exposure.
Implications:
- Early recognition of PBV allergy is vital, particularly for patients undergoing repeat SLNB procedures.
- Referral to specialist drug allergy services is recommended for comprehensive evaluation of suspected PBV allergy.
- Improved diagnostic strategies and patient management are needed to mitigate risks associated with PBV in medical settings.
Related Concept Videos
Allergic Reactions: Anaphylaxis
Anaphylaxis is a severe, life-threatening hypersensitivity reaction mediated by Immunoglobulin E (IgE) antibodies. When IgE binds to allergens, it triggers the release of mediators– histamine, leukotrienes, and prostaglandins from mast cells and basophils. These mediators cause vasodilation, edema, and inflammation, leading to various symptoms.The primary allergens causing anaphylaxis include food items (e.g., peanuts, shellfish), drugs (e.g., penicillin, asparaginase, corticotropin, heparin),...
Allergic Reactions
Overview
Drug Toxicity: Allergic Reactions
Drug-related allergies are immune-mediated responses triggered by the administration of pharmacological agents. These hypersensitivity reactions are classified based on the immune mechanisms involved. The four primary types—Type I, II, III, and IV—are mediated by different immunological pathways and exhibit distinct clinical manifestations.Type I Hypersensitivity/ IgE-Mediated Reactions: Immunoglobulin E (IgE) immediately mediates Type I hypersensitivity reactions. Upon initial exposure to a...
Allergic Drug Reactions
Allergic reactions related to drugs are hypersensitivity responses driven by the immune system and bear no connection to the drug's therapeutic action. While drugs in isolation do not trigger an immune response, they can interact with endogenous proteins to form antigens. These antigens stimulate lymphocytes to produce antibodies. IgE-type antibodies attach themselves to mast cells. Upon subsequent exposure to the same stimulus, the antigen-antibody interaction is initiated, unleashing numerous...
Pharmaceutical Poisoning: Potential Scenarios
Pharmaceutical poisoning can occur through various channels, impacting an estimated 2 million hospitalized patients in the U.S. annually with serious adverse drug responses. These scenarios encompass both therapeutic uses, such as drug toxicity, where even standard dosages can lead to severe central nervous system depression, and non-therapeutic exposures, including accidental ingestion by children, and environmental and occupational exposures.Unintentional poisonings often involve exploratory...
Pharmacovigilance
Post-marketing surveillance is a critical component of pharmaceutical regulation, often uncovering unanticipated adverse drug reactions (ADRs) once a drug is widely used over an extended period.
This process, termed pharmacovigilance, aims to detect, evaluate, and minimize harmful effects related to medication use. The data collection for pharmacovigilance depends on spontaneous reporting systems, where healthcare professionals or patients voluntarily report suspected ADRs.
In some cases, there...
This process, termed pharmacovigilance, aims to detect, evaluate, and minimize harmful effects related to medication use. The data collection for pharmacovigilance depends on spontaneous reporting systems, where healthcare professionals or patients voluntarily report suspected ADRs.
In some cases, there...

