Porphyria Overview 

Porphyria Overview 

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Porphyria is named from the ancient Greek word porphura, meaning purple. [1] Porphyrins are precursors of heme, a part of the hemoglobin molecule. Heme is manufactured in a multistep process. Defects of enzymes needed at various steps of heme synthesis result in distinct clinical syndromes known as porphyrias. [2] These syndromes can be clinically classified into those predominantly involving the skin, those manifesting as disorders of the liver/nervous system, and a combination involving all three entities (see the image below).

Porphyrias can be inherited or (rarely) acquired. [3] With the exception of congenital erythropoietic porphyria (CEP), which is autosomal recessive, all other porphyrias are inherited as autosomal dominant disorders. They invariably result in accumulation and increased excretion of porphyrins and their precursors. Some porphyrias have acute presentations (acute intermittent, variegate, hereditary coproporphyria), whereas others have a chronic, relatively stable presentation (congenital, erythropoietic). [4]

King George III of England had symptoms of abdominal pain, rashes, reddish urine, and psychotic episodes that are consistent with porphyria, although the account is disputed by many. [5] During the period 1955-1959, approximately 4000 people in southeast Anatolia (Turkey) developed porphyria due to the ingestion of hexachlorobenzene (HCB), a fungicide that was added to wheat seedlings. [6]

Urine and stool studies in various types of porphyria are summarized in the image below.

Heme synthesis is summarized in the image below. In some porphyria patients and families, however, diagnostic evaluation can reveal simultaneous findings that are compatible with two different forms of porphyria, a phenomenon referred to as dual porphyria. [7]

Porphyrias present in 2 distinct syndromes, acute and chronic.

The acute porphyrias are characterized by periodic acute attacks of neurovisceral symptoms and may stay occult for a long time. Four major disorders in this group are as follows:

  These porphyria syndromes are characterized by abdominal pain, neurologic deficits, psychiatric symptoms, and colored (red) urine.

The chronic porphyrias are dermatologic diseases that may or may not involve the liver and nervous system and do not present with acute attacks as described for the acute porphyrias above. These syndromes include congenital erythropoietic porphyria, erythropoietic porphyria, and porphyria cutanea tarda.

Clinical manifestations depend on the step in which the enzymatic defect occurs. If the enzymatic defects are in the initial steps of the metabolic cascade, early metabolic intermediates will accumulate (ie, aminolevulinic acid [ALA] and porphobilinogen [PBG]), which are responsible for attacks of neurologic dysfunction.

Overproduction of the heme precursor delta-aminolevulinic acid is the cause of pain in the acute porphyrias; inhibition of hepatic delta-aminolevulinic acid synthase-1, the enzyme that catalyzes delta-aminolevulinic acid formation, is key to the therapeutic efficacy of hemin infusion. [8] If the enzymatic defects are in the final steps, sunlight-induced cutaneous lesions (photosensitivity) due to porphyrin accumulation in the skin will develop. [9]

Doss porphyria, also known as plumboporphyria (ALA dehydratase deficiency), is extremely rare. [10] Abdominal pain and polyneuropathy are typical of this syndrome. Urinary ALA and coproporphyrin are markedly increased. Molecular genetic studies of the ALA dehydratase gene reveal the mutated nucleotides. In some patients, the development of the acute porphyria syndrome while the patient received pharmacologic doses of erythropoietin, which resolved when the drug was stopped, suggests that by stimulating heme synthesis, erythropoietin may unmask an enzyme deficiency resulting in the clinical expression of ALA dehydratase deficiency porphyria. [11] . Sometimes, exposure to lead may unmask occult plumboporphyria. [12]

Acute porphyria attacks are brought about by uncontrolled upregulation of the ALA synthase enzyme. This can be precipitated by certain lipophilic drugs (see the Drugs to Avoid section), hypoglycemia (“the glucose effect”), [13] and a deficiency of heme, the end-product of the heme pathway (see the image below) that acts as a negative feedback mechanism in normal circumstances. [14, 15, 16, 17]

Hereditary coproporphyria results in most cases from half-normal activity (50%) of coproporphyrin oxidase. [18] The disease is an acute hepatic porphyria that is characterized by abdominal pain, neuropsychiatric symptoms, and cutaneous photosensitivity [19] In rare homozygous cases, enzyme activity decreases to < 10% and the term harderoporphyria is used. [20]

Variegate porphyria is an autosomal dominant inherited trait that results in decreased activity of protoporphyrinogen oxidase. It is characterized clinically by photosensitive skin disease and a propensity to acute neurovisceral crises. It presents with chronic blistering skin lesions that are less prevelant in colder regions and dark-skinned individuals. [21] Variegate porphyria is found worldwide but has an exceptionally high frequency in South Africa. [22]

Erythropoietic protoporphyria (EPP) is caused by loss-of-function mutations in the ferrochelatase (FECH) gene. [23] In EPP, the protoporphyrin molecule accumulates and can be excited by absorbing light energy. This causes the generation of free radicals and, thereby, photosensitivity of all tissues exposed to light. Mechanisms of toxicity in tissues not exposed to light include the following:

Clinical manifestations of EPP are photosensitivity, insignificant hematologic abnormalities, and liver disease. [24] The hepatic manifestations of the disease are diverse: mildly disturbed liver enzymes in 20% to fatal hepatic failure in less than 5%. [25]

Porphyria cutanea tarda (PCT) is characterized by the defective uroporphyrinogen III decarboxylase enzyme. There are 3 types of porphyria cutanea tarda with typical skin manifestations; patients present with skin fragility, erosions, vesicles, bullae, and milia in sun-exposed areas of the skin. Sometimes, there is the presence of periorbital mottled hyperpigmentation and hypertrichosis, sclerodermoid changes, and ulceration. [26]

Hemochromatosis gene (HFE) mutations and the hepatitis C virus (HCV) are both risk factors for PCT. In a French cohort of PCT patients with both C282Y and H63D were more frequent in PCT+ patients than in controls, but there was no difference in HFE genotype according to HCV seropositivity. [27] Up to two thirds of Saxon patients with PCT carry the classic HFE mutations (C282Y and/or H63D). PCT is associated with antibodies to HCV. PCT is an important extrahepatic manifestation of HCV-infection. [28] In a Swedish cohort, 38% of male patients with PCT had a history of alcohol abuse. [29]

Congenital erythropoietic porphyria (Gunther disease)

Congenital erythropoietic porphyria, or Gunther disease is one of the least common porphyrias. [30] It results from a deficient activity of uroporphyrinogen III synthase (URO-synthase). Clinical onset usually occurs in infancy or in early childhood, but very rare cases of onset at puberty or later have been reported. [31]   Hemolysis may be a feature in homozygous cases. [32] Prolonged exposure to sunlight may precipitate a blistering rash, red urine, and even blindness. [33, 34]

First described in 2008, this subtype is similar in presentation to erythropoietic protoporphyria but has a higher incidence of liver disease and higher levels of erythrocyte protoporphyrin, with an X-linked dominant inheritance pattern. [35]

The combined prevalence of the acute porphyrias is approximately 5 cases per 100,000 persons. [36] Porphyria cutanea tarda is the most common porphyria, with a prevalence of 1 in 10,000. The most common acute porphyria, acute intermittent porphyria, has a prevalence of approximately 1 in 20,000, and the prevalence of the most common erythropoietic porphyria, erythropoietic protoporphyria, is estimated at 1 in 50,000 to 75,000. [37] Congenital erythropoietic porphyria is extremely rare, with an estimated prevalence of 1 in 1,000,000 or less. [37] Fewer than 200 cases have been reported in the literature. [38]

A specialist porphyria center network (European Porphyria Network [EPnet]) estimated the risk of recurrent attacks at 4% of porphyria patients in Europe. The incidence of symptomatic porphyria was around 0.13 case per million per year in most European countries, except Sweden, where it was 0.51 case per million per year. [39, 40]

The most common presenting symptom (90%) of an acute porphyria is abdominal pain. [41] This is usually colicky in nature, located in the left lower abdomen, and lasts hours to days. The abdominal pain is rarely accompanied by fever, leukocytosis, or peritoneal signs. Nausea and vomiting appear common. [42]

There is a very characteristic discrepancy between the severity of the patient’s complaints and the objective clinical findings. [43] When a patient has repetitive visits to the emergency department because of severe abdominal pain without reasonable causes and needs narcotics for pain control, acute porphyria should be taken into consideration. [44]

Muscle weakness and focal neurologic deficits such as tetraparesis [45] may be the presenting feature, [46] especially in women of reproductive age. Limb pain is common. A motor, axon-predominant neuropathy is a strong clue when accompanied by abdominal and psychiatric symptoms. [47] A minority of patients present with paresis only, and no abdominal pain. [48]

The lifetime prevalence of acute intermittent porphyria–associated seizures has been reported as 2.2% of all those with known acute intermittent porphyria and 5.1% of all those with manifest acute intermittent porphyria. Epileptic seizures among persons with acute intermittent porphyria are less common than has been previously described. [49]

Some patients develop psychiatric symptoms such as psychosis similar to schizophrenia. Diagnostic difficulty may lead to underdiagnosis of patients who present with strictly psychiatric symptoms. This assumption is supported by a high prevalence of acute intermittent porphyria in psychiatric hospitals. [50]

Anxiety is raised in patients with acute intermittent porphyria and with variegate porphyria, in males and females, compared with the normal population. [51]

Acute intermittent porphyria should be suspected in individuals presenting with unexplained acute abdominal pain following international air travel. [52]

The relative risk of an acute attack in acute intermittent porphyria compared with that in variegate porphyria was 14 in a series of 112 patients from South Africa with porphyria attack. [53]

A thorough family history for porphyria and the patient’s occupational history must be obtained.

In acute porphyrias presenting as abdominal pain, attention should be paid to peritoneal signs, which are typically absent in porphyria. The presence of localized tenderness, rebound tenderness, vaginal discharge, cervical motion tenderness, and/or genitourinary bleeding should raise “red flags” even in patients known to carry a diagnosis of porphyria, and alternative diagnoses should be sought.

Jaundice may or may not be present. [54]

A focused neurologic exam should be performed to identify motor and sensory deficits and peripheral neuropathy.

In some but not all acute porphyrias, a skin rash may be seen. Variegate porphyria and, much less commonly, hereditary coproporphyria can also cause chronic, blistering lesions on sun-exposed skin that are identical to those in porphyria cutanea tarda, a much more common condition.

Gross, biochemical, and microscopic examination of the patient’s urine is paramount if porphyria is on the differential diagnosis. The urine of patients with porphyria cutanea tarda is red to brown in natural light (red-wine urine) and pink to red in fluorescent light. [55]

The differential diagnosis in porphyria includes the following:

Acute abdomen

Hereditary tyrosinemia type I [56]

Lead poisoning

Pseudoporphyria is a bullous photosensitivity that most commonly arises as an adverse effect of a variety of medications, such as the antifungal agent voriconazole [57]


The clinical criteria of an acute attack of intermittent porphyria include the paroxysmal nature of the episode, the absence of other obvious causes, and the combination of various signs and symptoms, such as the following [58] :

The key manifestations that indicate possible acute porphyria are intensive abdominal pain without peritoneal signs; acute peripheral neuropathy; and encephalopathy, usually with seizures or psychosis. The presence of typical signs and symptoms, along with a more than fivefold elevation of urinary porphobilinogen excretion, justify starting treatment. [58]

Urine porphyrin studies are the mainstay in the diagnosis of acute porphyria attacks. Establish the diagnosis promptly by testing for increased porphobilinogen (PBG) in a single-void urine collected during an attack. An expert guidelines panel recommended the Trace PBG Kit [Thermo Trace/DMA, Arlington, Tex]. [41]  

Urine samples for PBG testing should be protected from light (eg, by wrapping the specimen container in aluminum foil or placing it in a brown paper bag). However, brief exposure to light will not compromise the test results. Urine study results are unreliable if the urine creatinine level is below 2 mmol/L. [59]

 Patients with acute exacerbations of porphyria have logarithmic increases (5-100 times) in metabolic precursors (eg, aminolevulinic acid [ALA], PBG). Minor elevations of these precursors are nondiagnostic and nonspecific. [60]

Significantly increased ALA and PBG in urine have 100% specificity (ie, rules in) for acute intermittent (hepatic) porphyria, variegate porphyria, and coproporphyria. A normal urine PBG result has a sensitivity of almost 100% (ie, rules out) in the diagnosis of porphyria in acutely symptomatic patients. [61]

To assess for cutaneous porphyria, the plasma porphyrin level should be measured, using fluorescence emission spectroscopy.  Whole blood for porphyrin analysis is used to identify protoporphyria plasma porphyrins. [59]


Stool coproporphyrin and protoporphyrin are the most commonly measured porphyrins in feces. The ratio of fecal coproporphyrin to fecal protoporphyrin varies among the porphyrias. For example, fecal protoporphyrin always exceeds coproporphyrin (P > C = V) in variegate porphyria, whereas the reverse is true in hereditary coproprophyria. [62]

Erythrocyte uroporphyrinogen decarboxylase activity is a specific and intrinsic defect in porphyria cutanea tarda; measurement of this enzyme is a reliable diagnostic test for this disease. [63]

Hyponatremia is typical. [64] In 1966, lesions of the median eminence of the hypothalamus and both hypothalamic–hypophyseal tracts were described in a patient with acute intermittent porphyria and syndrome of inappropriate antidiuretic hormone (SIADH). It was suggested that SIADH occurred because of damage to these areas of the brain from excessive exposure to porphyrins. [65]

Genetic mutations are increasingly available for testing in the diagnosis of porphyrias. Prenatal diagnosis is possible in some types of porphyria.

For example, in congenital erythropoietic porphyria, pink fluorescence of the amniotic fluid examined fortuitously in sunlight is suggestive. DNA analysis may show the mutation C73R in the gene for URO-synthase. [66] Another detectable mutation is PPOX encoding mitochondrial enzyme protoporphyrinogen oxidase in variegate porphyria. [21] Heterozygous mutation in CPOX (encoding coproporphyrinogen-III oxidase confirms the diagnosis of hereditary coproporphyria. [67] However, the utility of prenatal testing is questionable as many heterozygous carriers live healthy lives. The prenatal testing thus should not be done unless pregnancy termination is being considered.

A mutation screening for family members should be conducted to identify symptom-free carriers, especially in cases in which there is a positive family history. [45]

Computed tomography (CT) scanning of the abdomen and pelvis

CT scanning helps clinicians to rule out other diagnoses of excruciating abdominal pain, such as a ruptured viscus or vessel, and may help to pick up concomitant pathology, such as intussusception or infarction. [68] Focal, fatty nodularity of the liver may be noted in some patients. [69]

MRI of acute intermittent porphyria demonstrates multiple large, contrast-enhancing, subcortical white matter lesions, which regress with glucose and hematin infusions. Diffusion-weighted MRI is normal, and MR spectroscopy excludes acute demyelination or tissue necrosis. MRI findings of acute intermittent porphyria can differ from those in posterior reversible encephalopathy syndrome by virtue of intense contrast enhancement. Because diffusion-weighted MRI and MR spectroscopy are normal, the lesions are likely caused by reversible vasogenic edema and transient breakdown of the blood-brain barrier. [70]

T2-weighted MRI sequences demonstrated multiple white-matter, high-signal lesions in 4 of 16 acute intermittent porphyria gene carriers (25%). [71] Kupferschmidt and colleagues [72] described 2 patients with acute intermittent porphyria who presented with cortical blindness. MRI showed bilateral occipital lesions, and the investigators speculated that these lesions were caused by vasospasm-induced ischemia due to unopposed cerebral vasoconstriction that resulted from a deficiency of nitrous oxide synthase, a major vascular dilator.

The striking feature of the MRI findings in these cases and in those of acute intermittent porphyria described in the literature is that the lesions are bioccipital and partially or totally reversible. These characteristics are typical of MRI findings seen in patients with hypertensive encephalopathy, and many patients presenting with acute intermittent porphyria attacks have high blood pressure on presentation. [73]

In cases of porphyria cutanea tarda, MRI of the liver shows poorly defined areas, which, on T2-weighted sequences, exhibit a hypersignal with fat saturation. Treatment of porphyria cutanea tarda may lead to clinical remission and resolution of radiologic abnormalities. [74]

Therapeutic measures include the following:

Withdrawal of any culprit medications, alcohol, drugs, toxins, and chemicals is the key to therapy; smokers should be extensively counseled about cessation

Supportive care such as fluid, electrolytes, and nutrition is paramount

Monitor for hyponatremia or hypomagnesemia, and treat vigorously if found

Aggressively treat respiratory failure, which may ensue once muscle weakness involves the diaphragm, and support ventilation in an intensive care unit as appropriate

Treat pain with parenteral narcotics; complicated and debilitating chronic cases may require celiac plexus injection [75]

Administer phenothiazines for manifestations such as nausea, vomiting, agitation; ondansetron or related drugs can also be used for nausea [21]

Treat tachycardia and/or hypertension with propranolol or nadolol, which can be safely used for beta blockade once dehydration is ruled out

Promptly start glucose infusion in the form of 10% dextrose. At least 300-400 g should be given in 24 hours. The infusion is a time-buying measure to bridge the patient to more definitive treatment with hemin; by itself, glucose infusion is only effective for mild symptoms. [76]

Treat acute porphyria attacks with hemin (plasma-derived intravenous heme); 1-4 mg/kg/d for up to 14 days is the definitive treatment and mainstay of management. Both heme arginate and heme hydroxide have been used. [21] Thrombophlebitis is the major adverse effect. At least two thirds of patients have a good response, with resolution of pain and neurologic deficits. [77, 78, 79] Tin protoporphyrin appears to have a synergistic effect with hemin. [80]

Other therapies include the following:

Hemodialysis has been used in dire circumstances with some benefit when hemin was not available. [81]

Termination of pregnancy may have to be considered as a last resort in acute fulminant attacks presenting during pregnancy. [82]

Gonadotropin-releasing hormone (GdRH) analogues have been reportedly effective in some cases of acute intermittent porphyria, but these agents are not widely used. [83] They can be used to prevent acute attacks related to menstruation. [21]

Perioperative care should involve intravenous glucose and nonbarbiturate induction of anesthesia, as well as appropriate protection from intraoperative surgical lights with filters. [67]

Magnesium sulfate has been used to control seizures, as many regular antiseizure medications are contraindicated. [84]

Neither red blood cell exchange transfusion nor plasmapheresis prevented progressive hepatic deterioration in 2 cases of advanced hepatic erythropoietic protoporphyria despite a significant decrease in protoporphyrin levels. [85]

For acute hepatic porphyrias, in which attacks are caused induction of the enzyme 5-aminolevulinic acid synthase 1 (ALAS1), preclinical studies suggest that silencing of ALAS1 using small interfering RNA (siRNA) in a lipid nanoparticle can effectively prevents and treat attacks. [88]

Cutaneous porphyrias

The use of beta-carotene has shown some benefit for cutaneous porphyrias.

Porphyria cutanea tarda can be effectively treated by phlebotomy. [92] High-dose chloroquine therapy for porphyria cutanea tarda is rarely used now because of its adverse hepatic effects. [93] Low-dose chloroquine appears at least as effective as phlebotomy. [94]  A meta-anaysis found that relapse rates in the year following treatment were 20% with phlebotomy and 35-36% with chloroquine. [95]

Iron chelation therapy (eg, with deferasirox, deferiprone, or desferrioxamine) may be considered for patients with porphyria cutanea tarda if phlebotomy is contraindicated. In a pilot study of 10 patients with porphyria cutanea tarda, iron chelation with deferasirox reduced new blisters and ferritin levels in most patients. [96]

Afamelanotide, an α-melanocyte–stimulating hormone analogue, has been shown to permit increased duration of sun exposure without pain and improve quality of life in patients with erythropoietic protoporphyria. [97] It is administered in a subcutaneous implant containing a 60-day supply of the medication. Afamelanotide is not yet approved for marketing in the United States.

Congenital erythropoietic porphyria

Pharmacological chaperone molecules and gene therapy are being investigated in congenital erythropoietic porphyria. [104]

Of 206 adult Finnish patients with acute intermittent porphyria or variegate porphyria, 47 patients had a total of 117 acute attacks during the period of 1967-1989. [105] Six of these patients died during an attack, and 21 attacks were associated with paresis; the frequency of severe attacks was significantly smaller than before 1967. Most pareses and deaths occurred because of a delay in diagnosis and inappropriate treatment of porphyria.

In cases of acute intermittent porphyria, the risk of attacks correlated with the excretion of PBG in the urine during remission among adults; a low rate of excretion predicted freedom from acute attacks. Two percent of the surgical operations and 4% of the pregnancies were associated with acute attacks. Nearly one third of the women had symptoms of porphyria associated with the menstrual cycle, but these seldom proceeded to an acute attack. Forty-six percent of the women had used sex-hormone preparations regularly; 2 (4.5%) of the women experienced associated acute attacks.

Long-term complications in patients with acute intermittent porphyria include chronic hypertension, chronic kidney insufficiency, chronic pain syndrome, and hepatocellular carcinoma. [58] Patients with variegate porphyria have also shown increased incidences of hepatocellular carcinoma. [105]  

In patients with acute hepatic porphyria, Baravelli et al reported a substantially higher risk for primary liver cancer, with risk greater in women than in men. In addition, a meta-analysis by these authors suggested an association between acute hepatic porphyria and  increased risks of kidney cancer and endometrial cancer. [106]

Erythropoietic porphyria is a persistent, severely painful, socially disabling disease with a marked impact on quality of life. [107]

Educate patients about their porphyria disease, inheritance, precipitating drugs and events, and the importance of seeking treatment in early stages of an attack. [108]

Encourage patients to wear medical alert bracelets. [41]

Patients who smoke should be strongly encouraged to quit. Smoking, which increases hepatic cytochrome P450 enzymes and presumably heme synthesis, is associated with more frequent porphyria attacks. [109]

Perioperative management includes the use of filters on operative lights to prevent skin burns and intestinal perforation. [110] To prevent burn injuries, astral lamps in the operating room are covered with yellow film filters. [111]

A high risk of primary hepatocellular carcinoma has been demonstrated in acute hepatic porphyrias, and periodic surveillance is recommended. [112]

A listing of experts, testing, and centers of excellence in the porphyrias is available at the American Porphyria Foundation Website (www.porphyriafoundation.com).

The European Porphyia Initiative (EPI) (www.porphyria-europe.org) network was formed in 2001 to compare the experience among countries in an attempt to develop a common approach to the management of the porphyrias. [113]

The list of drugs to avoid continues to grow. Major culprits include the following:

Individual medications can be checked against a safe and unsafe drug database that is maintained by the American Porphyria Foundation.

Acute intermittent porphyrias are rare complications of ovulation induction with clomiphene citrate, but these syndromes should be considered in patients who develop unexplained hyponatremia or neurovisceral symptoms. [114]

Different drugs in the same class may have different effects in the porphyrias. For example, although lidocaine should be avoided, bupivacaine or levobupivacaine provided successful and safe local anesthesia for dental procedures in 5 children with a diagnosis of latent acute intermittent porphyria or who had a family history of acute intermittent porphyria. [115]

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Muhammad A Mir, MD, FACP Assistant Professor of Medicine (Hematology, Blood/Marrow Transplant) Milton S Hershey Medical Center, Pennsylvania State University College of Medicine

Muhammad A Mir, MD, FACP is a member of the following medical societies: American College of Physicians, American Society of Hematology, American Society for Blood and Marrow Transplantation, American Society of Clinical Oncology

Disclosure: Nothing to disclose.

Gerald L Logue, MD Professor of Medicine, Head of the Division of Hematology, Vice Chairman for Education, Department of Medicine, University of Buffalo State University of New York School of Medicine and Biomedical Sciences

Gerald L Logue, MD is a member of the following medical societies: Alpha Omega Alpha, American Association for the Advancement of Science, American College of Physicians, American Society of Hematology, American Federation for Clinical Research

Disclosure: Nothing to disclose.

Francisco Talavera, PharmD, PhD Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference

Disclosure: Received salary from Medscape for employment. for: Medscape.

Ronald A Sacher, MBBCh, FRCPC, DTM&H Professor of Internal Medicine and Pathology, Director, Hoxworth Blood Center, University of Cincinnati Academic Health Center

Ronald A Sacher, MBBCh, FRCPC, DTM&H is a member of the following medical societies: American Association for the Advancement of Science, American Association of Blood Banks, American Clinical and Climatological Association, American Society for Clinical Pathology, American Society of Hematology, College of American Pathologists, International Society of Blood Transfusion, International Society on Thrombosis and Haemostasis, Royal College of Physicians and Surgeons of Canada

Disclosure: Nothing to disclose.

Emmanuel C Besa, MD Professor Emeritus, Department of Medicine, Division of Hematologic Malignancies and Hematopoietic Stem Cell Transplantation, Kimmel Cancer Center, Jefferson Medical College of Thomas Jefferson University

Emmanuel C Besa, MD is a member of the following medical societies: American Association for Cancer Education, American Society of Clinical Oncology, American College of Clinical Pharmacology, American Federation for Medical Research, American Society of Hematology, New York Academy of Sciences

Disclosure: Nothing to disclose.

Many thanks to Ms. Jennifer Miller of the editorial staff for her patience, guidance, and cooperation during the production of this manuscript.

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