Bandemia refers to an excess of band cells (immature white blood cells) released by the bone marrow into the blood. The ICD diagnosis code for bandemia is 288.66.

It is a signifier of infection (or sepsis) or inflammation.

Measurement of it can play a role in the approach to appendicitis.

The causes of SIRS are broadly classified as infectious or noninfectious. Causes of SIRS include:

- trauma

- burns

- pancreatitis

- ischemia

- hemorrhage

Other causes include:

- Complications of surgery

- Adrenal insufficiency

- Pulmonary embolism

- Complicated aortic aneurysm

- Cardiac tamponade

- Anaphylaxis

- Drug overdose

SIRS is frequently complicated by failure of one or more organs or organ systems. The complications of SIRS include:

- Acute lung injury

- Acute kidney injury

- Shock

- Multiple organ dysfunction syndrome

Pelger–Huët anomaly (pronunciation: [pel′gər hyo̅o̅′ət]) is a blood laminopathy associated with the lamin B receptor.

It is characterized by a white blood cell type known as a neutrophil whose nucleus is hyposegmented.

It is a genetic disorder with an autosomal dominant inheritance pattern. Heterozygotes are clinically normal, although their neutrophils may be mistaken for immature cells which may cause mistreatment in a clinical setting. Homozygotes tend to have neutrophils with rounded nuclei that do have some functional problems.

Is a benign dominantly inherited defect of terminal neutrophil differentiation as a result of mutations in the lamin B receptor gene. The characteristic leukocyte appearance was first reported in 1928 by Karel Pelger (1885-1931), a Dutch Hematologist, who described leukocytes with dumbbell-shaped bilobed nuclei, a reduced number of nuclear segments, and coarse clumping of the nuclear chromatin. In 1931, Gauthier Jean Huet (1879-1970), a Dutch Pediatrician, identified it as an inherited disorder.

It is a genetic disorder with an autosomal dominant inheritance pattern. Heterozygotes are clinically normal, although their neutrophils may be mistaken for immature cells, which may cause mistreatment in a clinical setting. Homozygotes tend to have neutrophils with rounded nuclei that do have some functional problems. Homozygous individuals inconsistently have skeletal anomalies such as post-axial polydactyly, short metacarpals, short upper limbs, short stature, or hyperkyphosis.

Identifying Pelger–Huët anomaly is important to differentiate from bandemia with a left-shifted peripheral blood smear and neutrophilic band forms and from an increase in young neutrophilic forms that can be observed in association with infection.