Category: L

  • Listeriosis

    What it is:

    Listeriosis is a serious infection caused by eating food contaminated with the bacterium Listeria monocytogenes and has recently been recognized as an important public health problem in the United States. 

    Symptoms:

    A person with listeriosis usually has fever, muscle aches, and sometimes gastrointestinal symptoms such as nausea or diarrhea. If infection spreads to the nervous system, symptoms such as headache, stiff neck, confusion, loss of balance, or convulsions can occur.

    Infected pregnant women may experience only a mild, flu-like illness; however, infection during pregnancy can lead to premature delivery, infection of the newborn, or even stillbirth.

    Associated foods:

    •  Listeria monocytogenes is found in soil and water, so vegetables can become contaminated from the soil or from manure used as fertilizer. 

    • Animals can carry the bacterium without appearing ill and can contaminate foods of animal origin such as meats and dairy products.

    •  The bacterium has been found in a variety of raw foods, such as uncooked meats and vegetables, as well as in processed foods that become contaminated after processing, such as soft cheeses and cold cuts at the deli counter.

    •  Unpasteurized (raw) milk or foods made from unpasteurized milk may contain the bacterium.

    •  Listeria is killed by pasteurization, and heating procedures used to prepare ready-to-eat processed meats should be sufficient to kill the bacterium; however, unless good manufacturing practices are followed, contamination can occur after processing.

    Prevention:

    •  General recommendations:

    •  Cook thoroughly raw food from animal sources, such as beef, pork, or poultry.

    •  Wash raw vegetables thoroughly before eating.

    •  Keep uncooked meats separate from vegetables and from cooked foods and ready-to-eat foods.

    •  Avoid raw (unpasteurized) milk or foods made from raw milk.

    •  Wash hands, knives, and cutting boards after handling uncooked foods.

    •  Recommendations for persons at high risk, such as pregnant women and persons with weakened immune systems, in addition to the recommendations listed above:

    •   Avoid soft cheeses such as feta, Brie, Camembert, blue-veined, and Mexican-style cheese. (Hard cheesed, processed cheeses, cream cheese, cottage cheese, or yogurt need not be avoided.)

    •   Cook until steaming hot left-over foods or ready-to-eat foods, such as hot dogs, before eating.

    Although the risk of listeriosis associated with foods from deli counters is relatively low, pregnant women and  immunosupressed persons may choose to avoid these foods or thoroughly reheat cold cuts before eating.

    Treatment:

    Even with prompt treatment, some infections result in death. This is particularly likely in the elderly and in persons with other serious medical problems. When infection occurs during pregnancy, antibiotics given promptly to the pregnant woman can often prevent infection of the fetus or newborn.  Babies with listeriosis receive the same antibiotics as adults, although a combination of antibiotics is often used until physicians are certain of the diagnosis.

    People at risk:

    •  Pregnant women – They are about 20 times more likely than other healthy adults to get listeriosis.

    •  Newborns – Newborns rather than the pregnant women themselves suffer the serious effects of infection in pregnancy. 

    • Persons with weakened immune systems 

    • Persons with cancer, diabetes, or kidney disease

    •  Persons with AIDS – They are almost 300 times more likely to get listeriosis than people with normal immune systems.

    •  Persons who take glucocorticosteroid medications

    •  The elderly

  • Lupus

    Systemic Lupus Erythematosus:  A chronic inflammatory
    disorder of the connective tissue, it affects multiple organ systems ,
    as well as the skin and can be fatal.  It’s characterized by recurring
    remissions and exacerbation.  Exacerbation’s are especially common
    during the spring and summer.  Early detection and treatment is essential
    and prognosis improves, but patients may develop cardiovascular, renal
    or neurologic complications or severe bacterial infections.  This
    disorder strikes women more than men.

    Cause:  Studies shows that it is interrelated immunologic,
    environmental, hormonal, and genetic factors as  possible causes. 
    Risk factors may be due to viral infections, exposure to sunlight or ultraviolet
    light, immunization, pregnancy,  abnormal estrogen metabolism., stress,
    streptococcal or viral infections, and may include genetic predisposition.

    Symptoms:

    Facial erythema (butterfly rash)

    Photosensitivity

    Nonerosive arthritis

    Discord rash

    Oral or nasopharyngeal ulceration

    Pleuritis

    Pericarditis

    Seizures

    Psychoses

    Patchy alopecia

    Aching

    Malaise

    Fatigue

    Low grade fever

    Chills

    Anorexia

    Weight loss

    Lymp node enlargement

    Abdominal pain

    Nausea and or Vomiting

    Diarrhea or constipation

    Irregular menstrual periods

    Treatment:

    For mild symptoms:  Nonsteroidal anti-inflammatory drugs, 
    Topical treatment for skin lesions.

    Refractory skin lesions are treated with intralesional corticosteroids
    or antimalarials, such as hydroxychloroquine and chloroquine..  These
    type of medications can cause retinal damage, such treatment requires ophthalmologic
    examination every 6 months.

    Corticosteroids.

     



    Discoid Lupus Erythematosus: 
    is a form of lupus erythematosus marked by chronic skin eruptions that,
    if untreated, can lead to scarring and permanent disfigurement.  About
    1 out of 20 patients with discoid lupus erythematosus later develops systemic
    lupus erythematosus. 

    Cause:  The exact cause is unknown,
    evidence suggest an autoimmune defect.

    Symptoms:

    Lesions are red, raised, scaling plaques, with
    follicular plugging and central atrophy.  The raised edges and sunken
    centers give them a coin like appearance.  Lesions can appear anywhere
    on the body, they usually erupt on the face, scalp, ears, neck, and arms
    or on any part of the body that’s exposed to sunlight..


    Hair may become brittle or may fall out in patches.

    Treatment:

    Tropical intralesional, or systemic medication

    Avoid prolonged exposure to sun, fluorescent
    lighting, or reflected sunlight.

  • Lung Abscess

    Lung Abscess:  Lung infection that is accompanied by
    pus accumulation and tissue destruction.  It often has a well defined
    border.  Anaerobic or aerobic bacteria can cause lung abscess. 
    Antibiotics has made the condition much less common now than formerly. 
    Poor oral hygiene with dental or gingival (gum) disease is strongly associated
    with putrid lung abscess.

    Symptoms:

    Cough – may produce bloody, purulent, or foul smelling sputum.

    Pleuritic chest pain

    Dyspnea (difficulty breathing)

    Excessive sweating -Diaphoresis

    Chills Fever

    Headache

    Malaise

    Weight Loss

    Crackles

    Diminished breath sounds

    Treatment:

    Prolonged antibiotic therapy

    Postural drainage may help discharge necrotic material into upper airways,
    where expectoration is possible.

    Oxygen therapy may be needed

    Poor therapeutic response requires resection of the lesion or removal
    of the diseased section of the lung. 

    All patients need rigorous follow up and serial chest X-rays.

  • Leukemia

    Leukemia:  a progressive, malignant disease
    of the blood forming organs, marked by distorted proliferation (the reproduction
    or multiplication of similar forms, especially cells) and development of
    leukocytes (WBC) and their precursors (something that precedes) in the
    blood and bone marrow.  It’s most common forms include acute lymphoblastic
    (lymphocytic)
    leukemia
    (ALL)
    , involving abnormal growth of lymphocyte precursors (lymphoblasts);
    acute
    myeloblastic
    (myelogenous) leukemia (AML), involving
    rapid accumulation of myeloid precursors (myeloblasts); and acute
    monoblastic
    (monocytic)
    leukemia, or Schilling’s
    type,
    involving marked increases in monocyte precursors (monoblasts).

    Acute leukemia is most common in children, and ranks 20th as a cause
    of cancer related deaths among people of all age groups. Untreated, acute leukemia invariably leads to death, usually the result
    of complications that result from leukemic cell infiltration of bone marrow
    or vital organs.  With treatment, prognosis varies. (Studies shows)-In
    acute lymphoblastic leukemia, treatment induces remissions in 90% of children
    (average survival time: 5 years) and in 65% of adults (average survival
    time: 1 to 2 years).  Children between ages 2 and 8 have the best
    survival rate – about 50% with intensive therapy.  In acute myeloblastic
    leukemia, the average survival time is only 1 year after diagnosis, even
    with aggressive treatment.  In acute monoblastic leukemia, treatment
    induces remissions lasting 2 to 10 months in 40% of children.  Adults
    survive only about 1 year after diagnosis, even with treatment.

    Causes:  The exact cause of acute leukemia is unknown. 
    Risk factors are thought to include some combination of viruses,, genetic
    and immunologic factors, and exposure to radiation and certain chemicals.

    Symptoms:

    Sudden onset of high fever/low grade fever

    Abnormal bleeding (example: nosebleeds, gingival bleeding, purpura,
    ecchymoses, petechiae)

    Bruising (even if it’s a minor trauma)

    Prolonged menses (females)

    Weakness

    Pallor

    Dyspnea

    Fatigue

    malaise

    Tachycardia

    Palpitations

    Abdominal or bone pain.

    Headache

    Treatment:

    Systemic chemotherapy 

    Chemotherapy varies with the specific disorder:

    Bone marrow transplant is now possible in some cases.

    Antibiotic therapy, antifungal, and antiviral drugs may be ordered.

    Transfusions 


    Chronic Myelogenous Myelocytic) Leukemia
    (CML):
      Known also as: Granulocytic Leukemia,
    produces abnormal overgrowth of granulocyte precursors (myeloblasts, promyelocytes,
    metamyelocytes, and myelocytes) in bone marrow, peripheral blood, and body
    tissues. 

    CML progresses in three distinct phases: 
    the insidious chronic phase, with anemia and bleeding abnormalities;
    an accelerated phase; and, eventually, the acute phase (blastic
    crisis), in with myeloblasts, the most primitive granulocyte precursors,
    proliferate rapidly.  This disease is invariably fatal. Studies shows
    average survival time is 3 to 4 years after onset of the chronic phase
    and 3 to 6 months after onset of the acute phase.

    Causes:  Just about 90% of patients
    with CML have the Philadelphia (Ph1) chromosome.  Radiation and carcinogenic
    chemicals may induces this chromosome abnormality.  Myeloproliferative
    diseases also seem to increase the incidence of this disease.  Also
    believe to be a cause is that of an unidentified virus.

    Symptoms:

    Anemia

    Fatigue

    Weakness

    Decreased exercise tolerance

    Pallor

    Dyspnea

    Tachycardia

    Headache

    Thrombocytopenia  (decrease in number of
    platelets in circulating blood – resulting in bleeding and clotting disorders,
    such as retinal hemorrhage, ecchymosis, hematuria, melena, bleeding gums,
    nosebleeds, and easy bruising).


    Hepatosplenomegaly (enlargement of the liver
    and spleen), with abdominal discomfort and pain.


    Sternal and rib tenderness

    Low grade fever

    Weight loss

    Anorexia

    Prolonged infection and ankle edema

    Treatment:

    Chemotherapy

    Radiation therapy

    Splenectomy (controversial)

  • Legionnaires’ Disease

    Legionnaires’ Disease  or Legionella
    pneumophila : 
    It derives its name and notoriety from the peculiar,
    highly publicized disease that struck 182 people ( 29 of whom died) at
    na American Legion convention in Philadelphia in July 1976.

    Legionnaires’ disease is an acute bronchopneumonia produced by a gram-negative
    bacillus.  This disease may occur epidemically or sporadically, usually
    in late summer or early fall.  Its severity ranges from a mild illness,
    with or without pneumonitis, to multilobar pneumonia, with a mortality
    as high as 15%.  Pontiac syndrome mimics Legionnaires’ disease but
    produces few or no respiratory symptoms, no pneumonia, and no fatalities,
    but it leaves the patient fatigued for several weeks.

    Cause:  Legionnaires’ disease bacterium (LDB), is an aerobic,
    gram-negative bacillus that probably is transmitted by an airborne route. 
    In may be spread through cooling towers or evaporation condensers in air-conditioning
    systems, in soil and excavation sites. (it is not spread from person to
    person).

    LDB, usually affects more often in men than in women and is most likely
    to affect:

    Middle aged and elderly persons

    Immunocompromised patients

    Patients with a chronic underlying disease

    Alcoholics

    Symptoms:

    Onset of the disease may be gradual or sudden

    After a 2 to 10 day  incubation period, nonspecific, prodromal
    signs and symptoms appear, including:

    Diarrhea

    Anorexia

    Malaise

    Diffuse myalgias and generalized weakness

    Headache

    Recurrent chills

    Unremitting fever ( which may develop within 12 to 48 hours with a
    temperature that may reach 105 degree F

    Cough – initially nonproductive but eventually may produce grayish,
    nonpurulent and occasionally blood streaked sputum.

    Nausea & vomiting

    May become disorientated, confused and may have mild temporary amnesia

    Pleuritic chest pain

    Tachypnea

    Dyspnea

    May experience bradycardia

    Patient who develop pneumonia may also experience hypoxia

    Other complication include hypotension, delirium, acute respiratory
    failure, renal failure, and shock (usually fatal).

    **  See your doctor promptly if you have the above symptoms.

    Treatment:

    Antibiotic therapy

    Antipyretics

    Fluid replacement

    May require oxygen therapy

  • Laryngitis

    Larynx:  the organ of voice; the air passage
    between the lower pharynx and the trachea, containing the vocal cords and
    formed by nine cartilages.

    Laryngitis:  inflammation of the larynx

    Acute laryngitis may occur as an isolated infection or as part of a
    generalized bacterial or viral upper respiratory tract infection. 

    Cause:  Acute laryngitis results from infection, excessive use
    of the voice, inhalation of smoke and or fumes, and aspiration of caustic
    chemicals.

    Chronic laryngitis results from upper respiratory tract infection such
    as, sinusitis, bronchitis, allergy, and nasal polyps. It is also associated
    with constant exposure to dust or other irritants, smoking, alcohol abuse,
    and mouth breathing.

    Symptoms: 

    Hoarseness

    Pain – especially when swallowing and or speaking

    Fever

    Dry cough

    Malaise

    Laryngeal edema

    Chronic laryngitis – A persistent cough

    Treatment:

    Resting the voice would be the primary treatment.

    Analgesics and throat lozenges for pain – for viral infection

    Antibiotic therapy – for bacterial infection

    May require hospitalization – for severe, acute laryngitis

    Occasionally, when laryngeal edema results in airway obstruction, a
    tracheotomy (incision of an opening into the trachea through the skin and
    the muscles of the neck) may be necessary.

    In chronic laryngitis, effective treatment must eliminate the underlying
    cause.

    Suggestion:  Patient should maintain adequate humidification by
    using a vaporizer or humidifier during the winter, by avoiding air conditioning
    during the summer (because it dehumidifies), by using medicated throat
    lozenges, and by not smoking.  Completing the prescribed antibiotic
    therapy.  Modification of predisposing habits.