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Author: Dr Sara de Menezes, Basic Physician Trainee, Alfred Health, Melbourne, Australia; Chief Editor: Hon A/Prof Amanda Oakley, Dermatologist, Hamilton, New Zealand, May 2016.
Introduction
Anaemia
Myeloproliferative disorders
Haematopoietic stem cell transplantation
Coagulation disorders
Inflammatory disorders associated with haematological disease
Adverse reactions to drugs
Haematological diseases are a diverse range of conditions affecting the constituents of blood. This includes disorders of the blood cells (red cells, white cells and platelets) and cancerous conditions affecting these blood cells. Skin signs of haematological disease described here are helpful in diagnosis and may also cause complications.
Anaemia can be the result of nutrient deficiencies, for example, iron, B12 or folate.
Skin manifestations are:
Haemolytic anaemia, for example, due to sickle cell anaemia, results from the destruction of red blood cells, which leads to additional symptoms:
The process by which blood cells are produced (haematopoiesis) gives rise to cells in either the lymphoid or myeloid lineage.
Polycythaemia vera is an example of a chronic myeloproliferative disorder of myeloid cells that results in an increased red cell mass.
Skin manifestations are:
Mast cell disease also arises from a myeloid disorder in which mast cells accumulate in different organs and tissues in the body. This can be broadly divided into cutaneous mastocytosis, which is more common in children, and systemic mastocytosis, which is more common in adults.
Skin manifestations are:
Leukaemia cutis is a rare manifestation of undiagnosed or previously treated myeloproliferative and lymphoproliferative disorders, eg acute myeloid leukaemia (AML), non-Hodgkin lymphoma. It is a result of infiltration of the skin by leukaemic cells, resulting in variable papules, nodules and plaques. Typically, they can be pinkish, violaceous (purplish) or darker than surrounding normal skin. In addition, they are almost always non-tender and palpable with a firm, indurated texture.
VEXAS syndrome is an acquired genetic condition seen in middle-aged men characterised by myelodysplastic haematological disorders and autoinflammatory features particularly involving the skin.
Lymphoproliferative disorders arise from disorders of stem cells of the lymphoid lineage. Systemic forms of lymphoma, Hodgkin lymphoma and non-Hodgkin lymphoma, may present with cutaneous signs. Specific cutaneous forms of lymphoma are described here.
Cutaneous T-cell lymphoma (CTCL) is a lymphoproliferative disorder that manifests mainly in the skin. The most common form of cutaneous lymphoma is mycosis fungoides.
Skin manifestations
Associated features include severe pruritus, hair loss, palmoplantar keratoderma (thickening of the skin of palms of hands/soles of feet) and secondary bacterial infection.
B-cell lymphomas can also present in the skin without evidence of spread elsewhere at the time they are diagnosed. These are known as primary cutaneous B cell lymphomas (PCBCL), including primary cutaneous marginal-zone lymphoma. Some of these are Epstein–Barr virus-associated lymphoproliferative disorders.
One particularly aggressive form of PCBCL is primary cutaneous large B cell lymphoma, leg type. Patients tend to be elderly and present with solitary or clustered, ulcerated, bluish, erythematous plaques or tumours located on the legs. This may be misdiagnosed as leg ulcers related to chronic venous insufficiency.
Multiple myeloma can rarely present with cutaneous plasmacytoma.
POEMS syndrome presents with Polyneuropathy, Organomegaly, Endocrinopathy, M protein and Skin changes. There is plasma cell proliferation and signs are mediated by overproduction of cytokines and other inflammatory markers.
Cryoglobulins are immunoglobulins that precipitate in cold temperatures. They result in palpable purpura and hyperviscosity syndrome with Raynaud phenomenon. Cryoglobulinaemia is classified as:
Cold agglutins are cold-sensitive immunoglobulins directed against antigens on red cells. They can lead to Raynaud phenomenon and acrocyanosis.
Amyloidosis refers to a group of protein-folding disorders where abnormal proteins are deposited in various tissues and organs, including the skin. The commonest of these is AL amyloidosis (light chain).
Skin manifestations
Stem cells for transplantation can be sourced from the blood, bone marrow or umbilical cord blood. Haematopoietic stem cell transplantation is an option to treat haematological malignancies where other treatment options have failed, for instance, diffuse large B cell lymphoma and myeloproliferative disorders.
Complications from haematopoietic stem cell transplantation can arise from side effects of immunosuppression, or from the person’s immune system attacking the ‘foreign’ donated cells (graft versus host disease, GVHD). Any organ in the body can be affected by acute or chronic GVHD (eg liver, lung, joints); however, the skin is most commonly affected.
Skin manifestations
Extracorporeal photopheresis (ECP) is used to treat cutaneous GVHD in stem cell transplant patients.
Disorders of coagulation result in either excessive blood clotting or excessive bleeding.
Disseminated intravascular coagulation (DIC) results in excessive clotting. It is triggered by severe infection, such as meningococcal disease, or illness, such as disseminated cancer. Severe DIC can consume all the clotting factors, which conversely leads to bleeding.
Skin manifestations are:
Thrombocytopenia leads to a bleeding tendency. For example in immune thrombocytopenia, platelet levels are reduced to a varying degree by circulating antibodies against them. Thrombocytopenia can also be due to bone marrow disease, Wiskott Aldrich syndrome and drugs.
Skin manifestations are:
Other coagulation disorders with cutaneous signs include:
Skin manifestations are:
Sweet syndrome (acute febrile neutrophilic dermatosis) is an acute inflammatory skin eruption that is accompanied by fevers and leukocytosis. It can be associated with infections, inflammatory bowel disease, haematological cancers and certain drugs (eg antibiotics). A localised variant of Sweet syndrome is known as neutrophilic dermatosis of the dorsal hands.
Skin manifestations
Drugs used to treat specific haematological conditions can have toxicities that manifest in the skin. Examples include: