ICD-10: B67.1

Echinococcus granulosus infection of lung

Additional Information

Description

Echinococcus granulosus infection of the lung, classified under ICD-10 code B67.1, is a specific type of echinococcosis caused by the parasitic tapeworm Echinococcus granulosus. This infection primarily affects the lungs but can also involve other organs, leading to a range of clinical manifestations.

Clinical Description

Pathophysiology

Echinococcus granulosus is a cestode (tapeworm) that typically resides in the intestines of definitive hosts, such as dogs and other canids. The life cycle involves the shedding of eggs in the feces of these hosts, which can then be ingested by intermediate hosts, including humans. Once ingested, the eggs hatch in the intestines, releasing larvae that penetrate the intestinal wall and migrate to various organs, most commonly the liver and lungs, where they form cysts.

Symptoms

The clinical presentation of Echinococcus granulosus infection in the lungs can vary significantly depending on the size and location of the cysts. Common symptoms include:

  • Cough: Often persistent and may be productive.
  • Chest Pain: Can be localized or diffuse, depending on the cyst's location.
  • Hemoptysis: Coughing up blood may occur if the cyst ruptures into the bronchial tree.
  • Dyspnea: Shortness of breath can result from cysts occupying lung space or causing pleural effusion.
  • Fever and Chills: These may occur, particularly if there is secondary infection or rupture of the cyst.

Diagnosis

Diagnosis typically involves a combination of clinical evaluation, imaging studies, and serological tests. Key diagnostic methods include:

  • Imaging: Chest X-rays and CT scans are crucial for visualizing cysts in the lungs. CT scans are particularly effective in assessing the size, number, and location of cysts.
  • Serological Tests: Blood tests can detect specific antibodies against Echinococcus granulosus, aiding in diagnosis.
  • Histopathological Examination: In some cases, tissue samples may be analyzed to confirm the presence of the parasite.

Complications

Complications can arise from untreated infections, including:

  • Cyst Rupture: This can lead to anaphylactic shock or secondary infections.
  • Pulmonary Abscess: Secondary bacterial infections may develop.
  • Pleural Effusion: Accumulation of fluid in the pleural space can occur.

Treatment

The management of Echinococcus granulosus infection of the lung typically involves:

  • Surgical Intervention: Surgical removal of cysts is often necessary, especially in cases of large or symptomatic cysts.
  • Medical Therapy: Antiparasitic medications, such as albendazole or mebendazole, may be used as adjunct therapy, particularly in inoperable cases or to reduce cyst size preoperatively.

Conclusion

Echinococcus granulosus infection of the lung (ICD-10 code B67.1) is a serious condition that requires prompt diagnosis and treatment to prevent complications. Awareness of the disease's clinical features and potential complications is essential for healthcare providers, especially in regions where echinococcosis is endemic. Early intervention can significantly improve patient outcomes and reduce the risk of severe complications associated with this parasitic infection.

Clinical Information

Echinococcus granulosus infection, particularly when it affects the lungs, is a significant health concern that can lead to various clinical manifestations. This condition is classified under ICD-10 code B67.1, which specifically denotes infections caused by Echinococcus granulosus, a parasitic tapeworm responsible for cystic echinococcosis (CE). Below is a detailed overview of the clinical presentation, signs, symptoms, and patient characteristics associated with this infection.

Clinical Presentation

Echinococcus granulosus primarily affects the liver and lungs, with pulmonary involvement being less common but clinically significant. The infection typically occurs through the ingestion of eggs from contaminated food or water, often linked to contact with infected dogs or their feces. Once ingested, the larvae migrate to various organs, forming cysts.

Signs and Symptoms

The clinical manifestations of Echinococcus granulosus infection in the lungs can vary widely, depending on the size and location of the cysts. Common signs and symptoms include:

  • Cough: A persistent cough is often one of the first symptoms, which may be dry or productive, depending on the presence of secondary infections.
  • Chest Pain: Patients may experience localized chest pain, which can be sharp or dull, often exacerbated by deep breathing or coughing.
  • Dyspnea: Shortness of breath can occur, particularly if the cysts are large enough to compress lung tissue or obstruct airways.
  • Hemoptysis: In some cases, patients may cough up blood, which can be alarming and indicative of cyst rupture or secondary infection.
  • Fever and Chills: Systemic symptoms such as fever may occur, especially if there is an associated infection or inflammation.
  • Weight Loss: Unintentional weight loss can be a sign of chronic infection or systemic illness.

Complications

Complications can arise from Echinococcus granulosus infection, including:

  • Cyst Rupture: This can lead to anaphylactic reactions or the spread of infection to other body parts.
  • Secondary Bacterial Infection: Ruptured cysts may become infected, leading to pneumonia or other respiratory complications.
  • Pleural Effusion: Accumulation of fluid in the pleural space can occur, leading to further respiratory distress.

Patient Characteristics

Certain demographic and clinical characteristics are commonly associated with patients suffering from Echinococcus granulosus infections:

  • Geographic Location: The prevalence of Echinococcus granulosus is higher in rural areas, particularly in regions where livestock farming is common, such as parts of South America, the Mediterranean, and Central Asia.
  • Occupational Exposure: Individuals working in agriculture, veterinary medicine, or those who have close contact with dogs are at increased risk.
  • Age: While the infection can occur at any age, it is often diagnosed in adults, particularly those aged 30-50 years.
  • Immunocompromised Status: Patients with weakened immune systems may be more susceptible to severe manifestations of the disease.

Diagnosis

Diagnosis of Echinococcus granulosus infection typically involves imaging studies such as ultrasound, CT scans, or MRI to identify cysts in the lungs and other organs. Serological tests can also be employed to detect specific antibodies against the parasite.

Conclusion

Echinococcus granulosus infection of the lung, classified under ICD-10 code B67.1, presents with a range of respiratory symptoms and can lead to significant complications if not diagnosed and treated promptly. Understanding the clinical presentation, signs, symptoms, and patient characteristics is crucial for healthcare providers to facilitate early diagnosis and effective management of this parasitic infection. Early intervention can significantly improve patient outcomes and reduce the risk of severe complications associated with this condition.

Approximate Synonyms

Echinococcus granulosus infection of the lung, classified under ICD-10 code B67.1, is a specific type of echinococcosis, which is a parasitic disease caused by the Echinococcus granulosus tapeworm. This condition primarily affects the lungs but can also impact other organs. Below are alternative names and related terms associated with this condition.

Alternative Names

  1. Cystic Echinococcosis: This term refers to the formation of cysts in various organs, including the lungs, due to the larval stage of Echinococcus granulosus. It is often used interchangeably with the specific lung infection when discussing the broader disease context.

  2. Hydatid Disease: This is a more general term that encompasses infections caused by Echinococcus species, including Echinococcus granulosus. It refers to the development of hydatid cysts in the body, which can occur in the lungs, liver, and other organs.

  3. Pulmonary Echinococcosis: This term specifically highlights the lung involvement in echinococcosis, emphasizing the respiratory system's role in the disease.

  4. Echinococcal Cyst of the Lung: This phrase describes the specific manifestation of the disease in the lung, focusing on the cystic structures formed by the parasite.

  1. Echinococcus granulosus: The specific species of tapeworm responsible for the infection, which is crucial for understanding the disease's etiology.

  2. Cysticercosis: While primarily associated with Taenia solium, this term is sometimes confused with echinococcosis due to the cystic nature of the infections. However, it is important to note that they are caused by different parasites.

  3. Zoonotic Infection: Echinococcus granulosus is a zoonotic parasite, meaning it can be transmitted from animals (often dogs and livestock) to humans, which is a significant aspect of its epidemiology.

  4. Echinococcal Disease: A broader term that encompasses all forms of echinococcosis, including those caused by Echinococcus multilocularis and Echinococcus granulosus.

  5. Cystic Echinococcosis of the Lung: This term is often used in medical literature to specify the location of the cysts within the lung, providing clarity in diagnosis and treatment discussions.

Conclusion

Understanding the alternative names and related terms for ICD-10 code B67.1 is essential for healthcare professionals, researchers, and students studying parasitic infections. These terms not only aid in accurate diagnosis and treatment but also enhance communication within the medical community regarding this significant health issue. If you have further questions or need more detailed information about echinococcosis, feel free to ask!

Diagnostic Criteria

Echinococcus granulosus infection, particularly in the lungs, is classified under the ICD-10 code B67.1. This condition, also known as cystic echinococcosis, is caused by the larval stage of the Echinococcus granulosus tapeworm. Diagnosing this infection involves a combination of clinical evaluation, imaging studies, and serological tests. Below is a detailed overview of the criteria used for diagnosis.

Clinical Criteria

  1. Patient History:
    - A thorough medical history is essential, including any exposure to dogs or environments where Echinococcus granulosus is endemic.
    - Symptoms may include cough, chest pain, hemoptysis (coughing up blood), and respiratory distress, which can indicate lung involvement.

  2. Physical Examination:
    - A physical examination may reveal signs of respiratory distress or abnormal lung sounds, which can suggest pulmonary involvement.

Imaging Studies

  1. Chest X-ray:
    - Initial imaging often includes a chest X-ray, which may show cystic lesions in the lungs. These lesions can appear as well-defined, round opacities.

  2. Computed Tomography (CT) Scan:
    - A CT scan is more definitive and can provide detailed images of the cysts, including their size, location, and any potential complications such as infection or rupture.
    - CT findings typically show cystic lesions with a characteristic "water-lily" sign or multiple cysts, which are indicative of Echinococcus infection.

  3. Magnetic Resonance Imaging (MRI):
    - In some cases, MRI may be used, especially if there is a need to assess the involvement of adjacent structures or to differentiate between cystic echinococcosis and other lung pathologies.

Serological Tests

  1. Echinococcus Antibody Testing:
    - Serological tests can detect antibodies against Echinococcus granulosus. Common tests include enzyme-linked immunosorbent assay (ELISA) and immunoblotting.
    - A positive serology test supports the diagnosis, although it is not definitive on its own, as false positives can occur.

  2. Specific Antigen Detection:
    - Advanced tests may involve detecting specific antigens related to Echinococcus granulosus, which can enhance diagnostic accuracy.

Differential Diagnosis

  • It is crucial to differentiate Echinococcus granulosus infection from other conditions that may present with similar symptoms or imaging findings, such as:
  • Tuberculosis
  • Lung abscesses
  • Neoplasms (tumors)
  • Other parasitic infections

Conclusion

The diagnosis of Echinococcus granulosus infection of the lung (ICD-10 code B67.1) relies on a combination of clinical history, imaging studies, and serological tests. Accurate diagnosis is essential for effective management and treatment, which may include surgical intervention or antiparasitic therapy. Given the potential for serious complications, timely diagnosis and treatment are critical in managing this infection.

Treatment Guidelines

Echinococcus granulosus infection, particularly when it affects the lungs, is a serious condition that requires careful diagnosis and treatment. This infection is classified under the ICD-10 code B67.1, which specifically refers to pulmonary echinococcosis. Below is a detailed overview of the standard treatment approaches for this condition.

Overview of Echinococcus Granulosus Infection

Echinococcus granulosus is a parasitic tapeworm that causes echinococcosis, primarily affecting the liver and lungs in humans. The infection occurs when a person ingests eggs of the parasite, often through contaminated food or water, or through contact with infected animals, particularly dogs. The larvae develop into cysts, which can grow in various organs, leading to significant health complications.

Diagnosis

Before treatment can begin, accurate diagnosis is crucial. This typically involves:

  • Imaging Studies: CT scans or MRI are commonly used to visualize cysts in the lungs and assess their size and number.
  • Serological Tests: Blood tests can help detect specific antibodies against Echinococcus granulosus, aiding in diagnosis.

Treatment Approaches

1. Surgical Intervention

Surgery is often the primary treatment for pulmonary echinococcosis, especially in cases where cysts are large or symptomatic. The surgical options include:

  • Cystectomy: Complete removal of the cyst, which is the preferred method when feasible.
  • Lobectomy: In cases where the cyst is extensive or involves significant lung tissue, a lobectomy (removal of a lobe of the lung) may be necessary.
  • Drainage: In some cases, percutaneous drainage of the cyst may be performed, especially if the cyst is infected or causing significant symptoms.

2. Medical Management

In addition to surgical options, medical treatment plays a crucial role, particularly in cases where surgery is not possible or as an adjunct to surgical intervention. The following medications are commonly used:

  • Albendazole: This antiparasitic medication is often prescribed to reduce the size of the cysts and prevent recurrence. It is typically administered for several weeks to months, depending on the severity of the infection.
  • Praziquantel: Another antiparasitic drug that may be used, although albendazole is more commonly preferred for echinococcosis.

3. Follow-Up and Monitoring

Post-treatment follow-up is essential to monitor for potential recurrence of the cysts. This typically involves:

  • Regular Imaging: Follow-up CT or MRI scans to assess the status of the lungs and check for new cyst formation.
  • Serological Testing: Periodic blood tests to monitor for the presence of antibodies against the parasite.

Conclusion

The management of Echinococcus granulosus infection of the lung (ICD-10 code B67.1) typically involves a combination of surgical and medical approaches tailored to the individual patient's condition. Early diagnosis and intervention are critical to prevent complications and improve outcomes. Regular follow-up is essential to ensure that the infection does not recur and to manage any long-term effects on lung function. If you suspect an infection or have been diagnosed, it is crucial to consult with a healthcare professional specializing in infectious diseases for appropriate management.

Related Information

Description

  • Echinococcus granulosus tapeworm infection
  • Primarily affects lungs but can involve other organs
  • Causes cough, chest pain, hemoptysis, dyspnea and fever
  • Diagnosed with imaging studies, serological tests and histopathology
  • Complications include cyst rupture, pulmonary abscess and pleural effusion
  • Treatment involves surgical removal of cysts or antiparasitic medications

Clinical Information

  • Pulmonary involvement is less common but clinically significant
  • Cough is often one of the first symptoms
  • Chest pain occurs in varying severity
  • Dyspnea can occur due to compressed lung tissue
  • Hemoptysis indicates cyst rupture or secondary infection
  • Fever and chills may accompany systemic illness
  • Weight loss is a sign of chronic infection
  • Cyst rupture leads to anaphylactic reactions or spread of infection
  • Secondary bacterial infection can occur after cyst rupture
  • Pleural effusion causes further respiratory distress
  • High prevalence in rural areas with livestock farming
  • Occupational exposure increases risk of infection
  • Adults aged 30-50 years are commonly diagnosed
  • Immunocompromised patients are more susceptible

Approximate Synonyms

  • Cystic Echinococcosis
  • Hydatid Disease
  • Pulmonary Echinococcosis
  • Echinococcal Cyst of the Lung
  • Zoonotic Infection
  • Echinococcal Disease
  • Cystic Echinoccosis of the Lung

Diagnostic Criteria

  • Thorough medical history including dog exposure
  • Clinical symptoms: cough, chest pain, hemoptysis
  • Respiratory distress or abnormal lung sounds on exam
  • Chest X-ray shows cystic lesions in lungs
  • CT scan confirms water-lily sign or multiple cysts
  • MRI may be used for adjacent structure assessment
  • Echinococcus antibody testing (ELISA, immunoblotting)
  • Specific antigen detection enhances diagnostic accuracy

Treatment Guidelines

  • Surgery often primary treatment option
  • Cystectomy preferred when feasible
  • Lobectomy may be necessary for large cysts
  • Drainage performed for infected or symptomatic cysts
  • Albendazole antiparasitic medication prescribed
  • Praziquantel used as alternative antiparasitic agent
  • Regular imaging and serological testing post-treatment

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