Immunodeficiency: Complications

The following are the major diseases or complications that may be contributed to by immunodeficiency or immunodeficiency:

Respiratory system (J00-J99)

  • Pneumonia (pneumonia)

Skin and subcutaneous (L00-L99)

Infectious and parasitic diseases (A00-B99).

  • Genital herpes
  • Scabies (scabies)
  • Tinea (dermatophytosis; fungal skin disease).

Neoplasms (C00-D48)

Special purpose code numbers (U00-U99).

  • Multi-resistant germs

Genitourinary system (N00-N99)

  • Balanitis (inflammation of the glans)
  • Colpitis / vaginitis (vaginitis).
  • Cystitis (cystitis)

In the following immunologic emergencies, immediate contact should be made with a clinic experienced in immunodeficiency diagnosis and treatment:

Symptoms or laboratory values Primary immunodeficiencies (PID)
Erythroderma (redness (erythema) of the entire skin organ) in the first weeks of life Suspected severe combined immunodeficiency (SCID): group of genetic diseases (autosomal or X-linked recessive genetic defects) characterized by a complete absence of immune defense (inhibition of T-lymphocyte development as well as, possibly. Absence of B lymphocytes and NK lymphocytes); if untreated, most affected individuals die in infancy; prevalence (frequency of disease) approximately 1:70,000
Severe lymphopenia in the 1st year of life Suspicion of severe combined immunodeficiency (see above).
Severe hypogammaglobulinemia Suspicion of severe combined immunodeficiency or agammaglobulinemia
Persistent fever, lymphoproliferation, and cytopenia (decrease in the number of cells in the blood); neurologic disturbances Suspicion of primary hemophagocytosis syndrome.
Severe neutropenia (decrease in neutrophil granulocytes) in infancy (<500/ l) Suspicion of severe congenital neutropenia.

Addresses of appropriate clinics can be found on the API homepage (www.kinderimmunologie.de) and the DGfI homepage (www.immunologie.de).