Difference between revisions of "HAEM5:Plasma cell neoplasms with associated paraneoplastic syndrome"

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==Cancer Category / Type==
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==WHO Classification of Disease==
  
[[HAEM4:Plasma Cell Neoplasms|Plasma Cell Neoplasm]]
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{| class="wikitable"
 
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!Structure
==Cancer Sub-Classification / Subtype==
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!Disease
 
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[[HAEM4:Plasma Cell Neoplasms with Associated Paraneoplastic Syndrome]]
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|Book
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|Haematolymphoid Tumours (5th ed.)
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|-
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|Category
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|B-cell lymphoid proliferations and lymphomas
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|Family
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|Plasma cell neoplasms and other diseases with paraproteins
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|-
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|Type
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|Plasma cell neoplasms
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|Subtype(s)
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|Plasma cell neoplasms with associated paraneoplastic syndrome
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==Definition / Description of Disease==
 
==Definition / Description of Disease==

Latest revision as of 17:34, 6 September 2024

Haematolymphoid Tumours (WHO Classification, 5th ed.)

editContent Update To WHO 5th Edition Classification Is In Process; Content Below is Based on WHO 4th Edition Classification
This page was converted to the new template on 2023-12-07. The original page can be found at HAEM4:POEMS Syndrome.

Other relevent pages include: HAEM4:TEMPI Syndrome

Note: author needs to include POEMS, TEMPI, and look for AESOP content

(General Instructions – The main focus of these pages is the clinically significant genetic alterations in each disease type. Use HUGO-approved gene names and symbols (italicized when appropriate), HGVS-based nomenclature for variants, as well as generic names of drugs and testing platforms or assays if applicable. Please complete tables whenever possible and do not delete them (add N/A if not applicable in the table and delete the examples); to add (or move) a row or column to a table, click within the table and select the > symbol that appears to be given options. Please do not delete or alter the section headings. The use of bullet points alongside short blocks of text rather than only large paragraphs is encouraged. Additional instructions below in italicized blue text should not be included in the final page content. Please also see Author_Instructions and FAQs as well as contact your Associate Editor or Technical Support)

Primary Author(s)*

Sohini Anand, MBBS

Tharanga Niroshini Senaratne, PhD

WHO Classification of Disease

Structure Disease
Book Haematolymphoid Tumours (5th ed.)
Category B-cell lymphoid proliferations and lymphomas
Family Plasma cell neoplasms and other diseases with paraproteins
Type Plasma cell neoplasms
Subtype(s) Plasma cell neoplasms with associated paraneoplastic syndrome

Definition / Description of Disease

POEMS syndrome is a rare blood disorder which is considered to be a subtype of plasma cell neoplasm. It is a multisystem disorder and stands for Polyneuropathy, Organomegaly, Endocrinopathy/edema, Monoclonal-protein (increased levels in blood), and Skin changes. In this condition, abnormal monoclonal proteins are secreted by plasma cells leading to its clinical presentations which include nerve damage, enlargement of spleen and/or lymph nodes, endocrine involvement leading to diabetes, thyroid abnormalities and certain skin/ hair changes such as hyperpigmentation, thickening of skin, red spots and increased facial hair growth.

Synonyms / Terminology

  • [1]Crow-Fukase syndrome
  • [1]Osteosclerotic myeloma
  • [1]PEP syndrome (Polyneuropathy-endocrinopathy-plasma cell dyscrasia syndrome)
  • [1]Shimpo syndrome
  • [1]Takatsuki syndrome[2]

Epidemiology / Prevalence

Not much information can be derived regarding the incidence and prevalence of POEMS syndrome.[Epidemiology 1]. Some information can be derived from the study conducted in Japan in the year 2015. The result showed that the prevalence is 0.3 per 1,00,000 with a male: female ratio of 1.5:1.[2] The median age of occurrence is 54.[3] However, few cases have also been seen in patients in their twenties.[1] Mean survival is 13.7 years.[4]

Clinical Features

Put your text here and fill in the table (Instruction: Can include references in the table. Do not delete table.)

Signs and Symptoms EXAMPLE: Asymptomatic (incidental finding on complete blood counts)

EXAMPLE: B-symptoms (weight loss, fever, night sweats)

EXAMPLE: Fatigue

EXAMPLE: Lymphadenopathy (uncommon)

Laboratory Findings EXAMPLE: Cytopenias

EXAMPLE: Lymphocytosis (low level)


editv4:Clinical Features
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As mentioned earlier, POEMS syndrome is a rare disorder which comprises of constellation of clinical presentations with neuropathy present in almost 100% of the cases. Following are the clinical features:

  • Polyneuropathy: One of the earliest presentations or may be the only presentation. The onset is usually sub-acute with mixed (sensory-motor) distal & symmetrical involvement. This is often associated with abnormal sensations like allodynia. Sensory involvement precedes motor loss. Most patients need assistance soon after developing polyneuropathy either because of loss of function or pain.[5]
  • Organomegaly and Organ dysfunction: There are multiple organ involvement and damage leading to organ dysfunction. Most common involved organs are lymph nodes, liver, kidney and spleen. Other organs which can be affected are CNS, renal, lung which can lead to asymptomatic parenchymal thickening, decreased GFR and pulmonary HTN; respectively. [5] Furthermore, arterial vascular involvement has been noted which can lead to cerebro-vascular accidents and ischemic strokes. [5]
  • Endocrinopathy: Multiple endocrinal organs can be involved. Most common presentation noted in males are erectile dysfunction because of hypogonadism which may be because of involvement of hypothalamus, pituitary or the primary organ itself(testes).[6] Other presentations can be diabetes, hypo/hyperthyroidism or adrenal gland abnormalities.
  • Monoclonal antibodies: POEMS syndrome is typically considered to be a plasma cell abnormality where plasma cells produce excessively high paraproteins particularly light chains (lambda proteins mainly of IgA type). The unique feature of POEMS which distinguish this condition from rest of the gammopathies is that- it is found that in approximately 50% of the pre-treatment specimens have reactive lymphoid aggregates which contain a mixture of both B and T cells with a thin rim of plasma cells. Other consistent finding are atypically appearing megakaryocytes with hyperplasia. Increased platelets counts are seen in 54% of the cases.[7] PBS is usually normal. [5]
  • Skin involvement: About 68% patients diagnosed with POEMS syndrome present with skin involvement. Most common is diffuse hyperpigmentation(purplish hue), acrocyanosis, calciphylaxis, thickening of skin, papular lesions, excessive sweating; aka; hyperhidrosis. Areas most commonly involved are extensor surfaces, neck, arm pit. Nail changes such as leukonychia. Hypertrichosis has also been reported. In few cases, hemangiomas such as cherry and capillary hemangiomas has been noted.
  • Other findings- fluid accumulation in body cavities leading to peritoneal effusion, pleural effusion and ascites.
  • Papilledema
  • Polycythemia
  • Specific finding in males- gynecomastia and impotence noted in male patients.
  • Specific findings in Females- amenorrhea and galactorrhea have been reported in female patients with POEMS syndrome

Sites of Involvement

POEMS syndrome involves multiple systems of the body.

  • Peripheral nerves and spinal cord: Peripheral neuropathy is present in 100% of the cases. This is the most common manifestation of POEMS syndrome.
  • Reticuloendothelial system- Lymph node, spleen and Liver are also most frequently involved. Lymph node simulates Castleman disease. Hepatosplenomegaly is present in almost 50% of the cases.
  • Bone- Bone is involved in 95% of the POEMS patient. Bone lesions are mostly sclerotic, but occasionally can be lytic lesions surrounded by thin rim of sclerosis. "Soap bubble" appearances have also been reported.[8]
  • Skin- About 90% of the POEMS patients develop skin changes. Most commonly being skin pigmentations.
  • Kidney- Kidney damage has been reported which can alter GFR and can lead to CKD.
  • Pancreas- Diabetes type2 has been noted.[9]
  • Adrenal gland- Involvement of adrenal glands cause malfunctioning leading to Addison's disease.[9]
  • Gonads- decreased level of testosterone can lead to hypo functioning of male gonads eventually leading to hypogonadism.[9]
  • Thyroids
  • Eye

Morphologic Features

  • Bone marrow Findings- Increased monoclonal plasma cells interspersed between polyclonal plasma cells with majority of monoclonal cells resembling λ chains. Plasma cell rimming around lymphoid aggregates. Also, Platelet precursors or megakaryocytes hyperplasia have been reported. [10]
  • Nerve fiber biopsies- POEMS syndrome has predilection for peripheral nerves compared to autonomic nerve fibers. The manifestation is severe and progressive. Biopsy specimens have shown 2 specific findings including axonal degeneration and epineural blood vessels formation which can be helpful in differentiating from C IDP(Chronic Inflammatory Demyelinating Polyradiculoneuropathy). CIDP presents as endoneurial inflammation and characteristic "onion bulb appearance".[11]
  • Skin Biopsies- Cases who developed hemangioma, biopsy showed "glomeruloid pattern"; accumulation of blood vessels containing RBCs in dilated vascular space resembling renal glomeruli. Patients who presented with skin thickening showed sclerosis with dilation of blood vessels on biopsy. Livedo reticularis biopsies showed thrombosis with necrosis in arterioles.[12]
  • Bone lesions biopsy: Osteosclerotic bone lesions biopsy shows proliferation of plasma cells which stain positive for CD138.[13]

Immunophenotype

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Finding Marker
Positive (universal) EXAMPLE: CD1
Positive (subset) EXAMPLE: CD2
Negative (universal) EXAMPLE: CD3
Negative (subset) EXAMPLE: CD4


editv4:Immunophenotype
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Plasma cells in BM biopsy ranges from<5% to 60%. 95% of the cases have value <5%.[14] Usually there are a combination of normal polyclonal plasma cells and monoclonal plasma cells. The monoclonal plasma cells stains positive for λ chains (IgA and IgG). [15]

POSITIVE

  • CD138+ forms plasma cell rim around lymphoid aggregates
  • CD38+ rim around lymphoid aggregates
  • monoclonal Plasma cells stains positive for cytoplasmic λ chain immunoglobulins.
  • Bright expression of CD45 and normal expression of CD19 in polytypic CD19 (Normal finding).
  • Lymphoid aggregates were staining positive for CD20+ B cells and CD3+ T cells.


NEGATIVE

  • Diminished expression of CD45 and loss of CD19 in monotypic plasma cells. (findings in POEMS).
  • κ chain immunoglobulin stain absent.
  • JAK2V617F mutation absent
  • HHV8 staining absent


Chromosomal Rearrangements (Gene Fusions)

Put your text here and fill in the table

Chromosomal Rearrangement Genes in Fusion (5’ or 3’ Segments) Pathogenic Derivative Prevalence Diagnostic Significance (Yes, No or Unknown) Prognostic Significance (Yes, No or Unknown) Therapeutic Significance (Yes, No or Unknown) Notes
EXAMPLE: t(9;22)(q34;q11.2) EXAMPLE: 3'ABL1 / 5'BCR EXAMPLE: der(22) EXAMPLE: 20% (COSMIC)

EXAMPLE: 30% (add reference)

Yes No Yes EXAMPLE:

The t(9;22) is diagnostic of CML in the appropriate morphology and clinical context (add reference). This fusion is responsive to targeted therapy such as Imatinib (Gleevec) (add reference).


editv4:Chromosomal Rearrangements (Gene Fusions)
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editv4:Clinical Significance (Diagnosis, Prognosis and Therapeutic Implications).
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  • Chromosomal Rearrangements (Gene Fusions)
  • Individual Region Genomic Gain/Loss/LOH
  • Characteristic Chromosomal Patterns
  • Gene Mutations (SNV/INDEL)

Diagnosis of POEMS syndrome requires meticulous search for clinical features and testing because of clinical simulation with other common conditions. Being one of the rare disease entities it can easily be missed by clinicians.

MANAGEMENT[7]

Management of POEMS syndrome requires multiple steps.

  1. Number one step is to determine baseline values-
  • history taking and physical examination- fundoscopy, skin examination, multiple organ assessments, neurological examinations.
  • Blood tests- CBC, hormone levels, VEGF, serum electrophoresis, quantitative immunoglobulins
  • Radiological assessments- skeletal surveys with CT/PET, organ assessments for effusion
  • Bone marrow biopsy of osteosclerotic lesions.
  • Systemic evaluation- kidneys- baseline 24 hour urine protein, urine electrophoresis, lung-PFTs, heart- Echocardiography, nerve electrophysiological studies and biopsies

2. 2nd step is to assess extent of bone marrow involvement-

SYSTEMIC THERAPY is considered in following conditions:

If iliac crest (IC) biopsy reports presence of plasma cells
If there is no plasma cells present in IC biopsy but more than 2 bony lesions are present. In disseminated lesions, systemic therapy may be needed.

Medications in systemic therapy includes- Melphalan, corticosteroids, cyclophosphamide-dexamethasone, lenalidomide-dexamethasone, proteasome inhibitors such as-Bortezomib.

RADIATION THERAPY:

If there are no plasma cells present in IC biopsy and there are less than 2 lesions present. Radiation therapy in these scenarios can be curative as well.

ASCT- Autologous stem cell transplant is considered to be 100% effective treatment.

Bevacizumab- is an anti-VEGF. It has been noted that the use of this medication has no superior effect over radiation and systemic therapy, although the main pathogenesis of POEMS syndrome is production of VEGF.


3. Supportive care - Supportive care is very important in POEMS syndrome. Physical therapy and/or occupational therapy improves short and long term complications such as contractures and improve muscle strength. Chest physiotherapy and CPAP (continuous positive airway pressure) improves lung function. Being a chronic progressive condition, physical and emotional support has a vital role in it's management.


MONITORING OF RESPONSE FOLLOWING THERAPY[7]

  • VEGF
  • M spike
  • PET SCAN for FDG SUVmax (clinical improvement when there is 50% reduction)
  • DLCO
  • improvement in papilledema
  • clinical improvement in effusions

Individual Region Genomic Gain / Loss / LOH

Put your text here and fill in the table (Instructions: Includes aberrations not involving gene fusions. Can include references in the table. Can refer to CGC workgroup tables as linked on the homepage if applicable. Do not delete table.)

Chr # Gain / Loss / Amp / LOH Minimal Region Genomic Coordinates [Genome Build] Minimal Region Cytoband Diagnostic Significance (Yes, No or Unknown) Prognostic Significance (Yes, No or Unknown) Therapeutic Significance (Yes, No or Unknown) Notes
EXAMPLE:

7

EXAMPLE: Loss EXAMPLE:

chr7:1- 159,335,973 [hg38]

EXAMPLE:

chr7

Yes Yes No EXAMPLE:

Presence of monosomy 7 (or 7q deletion) is sufficient for a diagnosis of AML with MDS-related changes when there is ≥20% blasts and no prior therapy (add reference).  Monosomy 7/7q deletion is associated with a poor prognosis in AML (add reference).

EXAMPLE:

8

EXAMPLE: Gain EXAMPLE:

chr8:1-145,138,636 [hg38]

EXAMPLE:

chr8

No No No EXAMPLE:

Common recurrent secondary finding for t(8;21) (add reference).

editv4:Genomic Gain/Loss/LOH
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A study conducted at Peking Union Medical college Hospital from November 2011 to June 2012 showed the following chromosomal abnormalities associated with POEMS syndrome.[16]. In this study, BM plasma cells CD138+ were collected using MACS system and then FISH technique was applied.

chromosomal translocation Genes in Fusion (5’ or 3’ Segments) Pathogenic Derivative Prevalence
14q32 [ t4,14( 33.3%), t11;14-(55.6%) IGHC/IGHV 45%
Chromosome Number Gain/Loss/Amp/LOH Region NAME %
13q14 loss Rb-1 25
1q12 Gain CEP-1 20

Characteristic Chromosomal Patterns

Put your text here (EXAMPLE PATTERNS: hyperdiploid; gain of odd number chromosomes including typically chromosome 1, 3, 5, 7, 11, and 17; co-deletion of 1p and 19q; complex karyotypes without characteristic genetic findings; chromothripsis. Do not delete table.)

Chromosomal Pattern Diagnostic Significance (Yes, No or Unknown) Prognostic Significance (Yes, No or Unknown) Therapeutic Significance (Yes, No or Unknown) Notes
EXAMPLE:

Co-deletion of 1p and 18q

Yes No No EXAMPLE:

See chromosomal rearrangements table as this pattern is due to an unbalanced derivative translocation associated with oligodendroglioma (add reference).

editv4:Characteristic Chromosomal Aberrations / Patterns
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Gene Mutations (SNV / INDEL)

Put your text here and fill in the table (Instructions: This table is not meant to be an exhaustive list; please include only genes/alterations that are recurrent and common as well as either disease defining and/or clinically significant. Can include references in the table. For clinical significance, denote associations with FDA-approved therapy (not an extensive list of applicable drugs) and NCCN or other national guidelines if applicable. Can also refer to CGC workgroup tables as linked on the homepage if applicable as well as any high impact papers or reviews of gene mutations in this entity. Do not delete table.)

Gene; Genetic Alteration Presumed Mechanism (Tumor Suppressor Gene [TSG] / Oncogene / Other) Prevalence (COSMIC / TCGA / Other) Concomitant Mutations Mutually Exclusive Mutations Diagnostic Significance (Yes, No or Unknown) Prognostic Significance (Yes, No or Unknown) Therapeutic Significance (Yes, No or Unknown) Notes
EXAMPLE: TP53; Variable LOF mutations

EXAMPLE:

EGFR; Exon 20 mutations

EXAMPLE: BRAF; Activating mutations

EXAMPLE: TSG EXAMPLE: 20% (COSMIC)

EXAMPLE: 30% (add Reference)

EXAMPLE: IDH1 R123H EXAMPLE: EGFR amplification EXAMPLE:  Excludes hairy cell leukemia (HCL) (add reference).


Note: A more extensive list of mutations can be found in cBioportal (https://www.cbioportal.org/), COSMIC (https://cancer.sanger.ac.uk/cosmic), ICGC (https://dcc.icgc.org/) and/or other databases. When applicable, gene-specific pages within the CCGA site directly link to pertinent external content.


editv4:Gene Mutations (SNV/INDEL)
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A study was conducted in 20 patients of POEMS syndrome. The study showed 7 gene shaving recurrent somatic gene mutations involved in POEMS syndrome. It is important to know that none of the important gene mutations involved in MM such as NRAS, KRAS, BRAF, and TP53 were found in POEMS syndrome patients.[17] HAEM4:Plasma Cell Neoplasms


The method used to find out the gene mutations were-

  • WES(Whole Exome Sequencing)- WES was performed in 20 patients. The mean depth in WES was 140x
  • Targeted Sequencing- TS was performed in all 20 patients. The mean depth in TS was 620x in more than 95% patients
  • Deep analysis of hot spots.
PROPERTIES OF GENES INVOLVED IN POEMS SYNDROME
Somatic genes mutations % Type of mutations 20 MUTATIONS LOCATION
KLHL6 20 MISSENSE MUTATION
  • R559Q
  • L71R
  • A91D
  • L258P
BTB

BACK


kelch1

LTB 15
  • MISSENSE MUTATION
  • SPLICE-SITE MUTATION
  • Q51E
  • T56R
  • 163-1 G>C
TNF
EHD1 10
  • MISSENSE MUTATION
  • SPLICE-SITE MUTATION
  • G70D
  • 71_75 del
  • 404+2 T>A
Dynamin N


EFhand4

EML4 10 MISSENSE MUTATION
  • S68N
  • D243N
HELP
HEPHL1 10 MISSENSE MUTATION
  • A270V
  • V526I
cu oxidase 2/3
PCDH10 10 MISSENSE MUTATION
  • S464C
  • V565M
  • L782R
  • L397L
Pkinase
HIPK1 10 MISSENSE MUTATION
  • N530S
  • I682V
cadherine2/c2


Other involved gene mutations were- ANK3, ATRX, BTG, CTNNB1, DNAH11, DNAH9, DST, DUSP2, EP300, EPHA7, ERBB2, HIST1H4L, IGLL5, NCKAP5, PKHD1L1, PLD1, RP1L1, RYR1, RYR3, SRCAP, USH2A, ZFHX3, and ZFHX4.



SOMATIC MUTATIONS OF FOLLOWING GENES CAN LEAD TO DEVELOPMENT OF NEUROPATHY IN POEMS SYNDROME[18]
GENE CHROMOSOME LOCATION LOCATION AA changes Stability (Kcal/mol)
PDLIM5 4 94456293 p.V49G -3.085
SEC24B 4 109449420 p.T46M 0.387
ZFHX3 16 72958758 p.A463E -1.178
PACRG 6 163312833 p.N223S -1.098



Epigenomic Alterations

PDLIM 5 is considered to be a part of PDZ-LIM protein family. This protein is involved in neuronal development. PDLIM 5 binds to the inhibitors of DNA binding 2 protein leading to suppression of inhibitory activities and proliferation and/ or regeneration of nerve axons. Mutation in the genes expressing this protein lead to abnormal axon growth and degeneration. This can lead to peripheral neuropathy seen in POEMS syndrome.[18]

Genes and Main Pathways Involved

Put your text here and fill in the table (Instructions: Can include references in the table. Do not delete table.)

Gene; Genetic Alteration Pathway Pathophysiologic Outcome
EXAMPLE: BRAF and MAP2K1; Activating mutations EXAMPLE: MAPK signaling EXAMPLE: Increased cell growth and proliferation
EXAMPLE: CDKN2A; Inactivating mutations EXAMPLE: Cell cycle regulation EXAMPLE: Unregulated cell division
EXAMPLE:  KMT2C and ARID1A; Inactivating mutations EXAMPLE:  Histone modification, chromatin remodeling EXAMPLE:  Abnormal gene expression program
editv4:Genes and Main Pathways Involved
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PATHOGENESIS OF POEMS SYNDROME

Nothing much is known about the pathophysiology of POEMS syndrome. Nevertheless, It is being presumed that various pro-inflammatory cytokines may be playing a strong role leading to multiple system involvement.[19]

  • Pro-inflammatory markers concentrations are increased leading to wide spread inflammation. Some of them are- TNF- α (Tumor Necrotic Factor), IFN-γ ( Interferon γ), IL-1β, IL-2, IL-6 (Interleukins). The cause of increased levels of cytokines are not known, but it has been hypothesized that cytokines are secreted because of stimulation by λ IGs secreted by plasma cells or by the tumor itself.
  • Decreased level of anti-inflammatory cytokines- A decreased level of TGF-β (Transforming Growth Factor β) may lead to imbalance between the pro and anti inflammatory factors resulting in disastrous clinical representation.
  • Role of VEGF- Again, it is being hypothesized that VEGF (Vascular Endothelial Growth Factor) may lead to neovascularization leading to proliferation of small blood vessels. It is important to note that disease activity correlates with VEGF levels even more than M proteins.[14]
  • λ Immunoglobulins

Genetic Diagnostic Testing Methods

Diagnosis of POEMS syndrome is extremely important because clinical features simulate other common disorder leading to misdiagnoses. In order to avoid misdiagnoses, meticulously looking into the presentations is mandatory.[7]

To start with- Detailed history taking and physical examination are important to look for constellations of clinical features mentioned above. Peripheral polyneuropathy and monoclonal plasma cells expressing λ immunoglobulins should always be present to diagnose POEMS syndrome. POEMS syndrome can be considered as one of the differential diagnoses in patients who do not respond to standard treatment of CIDP. It is also important to distinguish POEMS syndrome from other plasma cells disorders such as MGUS and multiple myeloma.

  • Biochemical tests- VEGF (Vascular Endothelial Growth Factor) levels in serum and plasma. Usual cut off level of VEGF for diagnosis of POEMS syndrome is 1920 pg/ml and 200 pg/ml. N-terminal propeptide of Type I- collagen is consider as novel blood marker for POEMS syndrome with a cutoff value of 70ng/ml. CBC to look for RBC concentrations and platelet counts. TSH, FSH, T3/T4, cortisol levels should be measured.
  • Radiological examinations- CT scan, PET scans, echocardiography should be done to look for bony lesions, organomegaly and fluid accumulations in body cavities.
  • Bone marrow biopsies- should be considered to look for presence of plasma cells in the osteosclerotic bony lesions.
  • Nerve conduction studies and nerve biopsies should be considered.


Familial Forms

Put your text here (Instructions: Include associated hereditary conditions/syndromes that cause this entity or are caused by this entity.)

Additional Information

PROGNOSIS

POEMS syndrome is a chronic progressive disorder. It can be fatal if left untreated, therefore early diagnosis and prompt treatment is crucial.[20] Median survival is 13.7 years.

GOOD PROGNOSIS

  • Response to radiotherapy
  • Absence of clubbing and effusions.

POOR PROGNOSIS

  • Presence of clubbing (median survival- 2.6 years) and effusions (median survival 6.6 years)

Death usually occurs due to malnutrition or infection such as lung infection.


DIFFRENTIAL DIAGNOSES

  • CIDP- chronic idiopathic demyelinating polyneuropathy- clinical manifestations of CIDP and POEMS are similar. However, the pathophysiology are different which can be appreciated in nerve biopsy. Both being a demyelinating conditions, can delay the diagnosis and management of POEMS syndrome because patients are usually managed for CIDP. Failure to response to management of CIDP should prompt physicians to consider possibility of POEMS syndrome.
  • AL AMYLOIDOSIS - The clinical presentations of amyloidosis may simulate POEMS syndrome such as organomegaly, nerve damage etc, but biopsy helps differentiates GB syndrome from POEMS syndrome. In former, biopsy shows amyloid fibrils accumulation where as in POEMS syndrome, neovascularization can be seen because of increased VEGF titers.
  • GUILLAINE BARRE SYNDROME- A preceding history of respiratory or genitourinary infection is present in GB syndrome. In severe form, respiratory failure can occur due to paralysis of diaphragm. GB syndrome is a self-limiting and spontaneous resolution occurs in most cases where as POEMS syndrome is a chronic progressive condition without antecedent history of diarrhea or respiratory illness.[21]
  • MGUS (MONOCLONAL GAMMOPATHY OF UNDETERMINED SIGNIFICANCE)- MGUS has increased levels of M protein in serum. Systemic involvement is rarely seen in MGUS. However, polyneuropathy may be seen occasionally in MGUS.


How to differentiate POEMS syndrome from Multiple myeloma (MM)?

  • Studies have shown that the POEMS syndrome patients are relatively younger than MM.[22]
  • The λ immunoglobulins in POEMS syndrome are typically IgG or IgA which is present only in small quantities. These small quantities can be easily missed by serum protein electrophoresis, therefore immunofixation electrophoresis techniques are applied to detect immunoglobulins in POEMS syndrome, unlike multiple myeloma. Also, in POEMS syndrome plasma cells in bone marrow biopsy are fewer than multiple myeloma; approximately 2%. [22] Plasma cells are present in large quantities in MM.
  • The bony lesions in POEMS syndrome are osteosclerotic type and /or mixed osteosclerosis + osteolytic giving it a "soap bubble appearance" where as in multiple myeloma it's osteolytic type. Therefore, typical symptoms of bone pain and fracture are absent in POEMS syndrome which are the presenting symptoms of multiple myeloma. Radiological studies have shown normal FDG avidity in POEMS syndrome(osteosclerotic lesions) and high FDG avidity in multiple myeloma( osteolytic lesions)[22]
  • Polyneuropathy is rarely seen in MM. It can be present with MM when associated with amyloidosis.
  • CRAB - Hypercalcemia, renal insufficiency, anemia and osteolytic bone lesions which are characteristically present in MM are rarely seen in POEMS syndrome.[23]

Links

HAEM4:Plasma Cell Neoplasms with Associated Paraneoplastic Syndrome

References

(use the "Cite" icon at the top of the page) (Instructions: Add each reference into the text above by clicking on where you want to insert the reference, selecting the “Cite” icon at the top of the page, and using the “Automatic” tab option to search such as by PMID to select the reference to insert. The reference list in this section will be automatically generated and sorted. If a PMID is not available, such as for a book, please use the “Cite” icon, select “Manual” and then “Basic Form”, and include the entire reference.)

  1. 1.0 1.1 1.2 1.3 1.4 1.5 https://rarediseases.org/rare-diseases/poems-syndrome/
  2. 2.0 2.1 Suichi, Tomoki; et al. (2019-09-03). "Prevalence, clinical profiles, and prognosis of POEMS syndrome in Japanese nationwide survey". Neurology. 93 (10): e975–e983. doi:10.1212/WNL.0000000000008062. ISSN 1526-632X. PMID 31371568.
  3. Suichi, Tomoki; et al. (2019-09-03). "Prevalence, clinical profiles, and prognosis of POEMS syndrome in Japanese nationwide survey". Neurology. 93 (10): e975–e983. doi:10.1212/WNL.0000000000008062. ISSN 1526-632X. PMID 31371568.
  4. Marinho, Flauberto Sousa; et al. (2015). "Cutaneous Manifestations in POEMS Syndrome: Case Report and Review". Case Reports in Dermatology. 7 (1): 61–69. doi:10.1159/000381302. ISSN 1662-6567. PMC 4448059. PMID 26034475.CS1 maint: PMC format (link)
  5. 5.0 5.1 5.2 5.3 Brown, Rachel; et al. (2019). "POEMS syndrome: clinical update". Journal of Neurology. 266 (1): 268–277. doi:10.1007/s00415-018-9110-6. ISSN 0340-5354. PMC 6342878. PMID 30498913.
  6. Dispenzieri, Angela; et al. (2018-02). "POEMS Syndrome". Hematology/Oncology Clinics of North America. 32 (1): 119–139. doi:10.1016/j.hoc.2017.09.010. ISSN 0889-8588. Check date values in: |date= (help)
  7. 7.0 7.1 7.2 7.3 Dispenzieri, Angela (2019). "POEMS Syndrome: 2019 Update on diagnosis, risk-stratification, and management". American Journal of Hematology. 94 (7): 812–827. doi:10.1002/ajh.25495. ISSN 1096-8652.
  8. "POEMS Syndrome - an overview | ScienceDirect Topics".
  9. 9.0 9.1 9.2 "POEMS Syndrome - Hormonal and Metabolic Disorders".
  10. Dao, Linda N.; et al. (2011-06-16). "Bone marrow histopathology in POEMS syndrome: a distinctive combination of plasma cell, lymphoid, and myeloid findings in 87 patients". Blood. 117 (24): 6438–6444. doi:10.1182/blood-2010-11-316935. ISSN 1528-0020. PMC 3123015. PMID 21385854.
  11. Piccione, Ezequiel A.; et al. (2016-10-31). "Nerve pathologic features differentiate POEMS syndrome from CIDP". Acta Neuropathologica Communications. 4. doi:10.1186/s40478-016-0389-1. ISSN 2051-5960. PMC 5088652. PMID 27799073.
  12. Barete, Stéphane; et al. (2010-06-01). "Skin Manifestations and Vascular Endothelial Growth Factor Levels in POEMS Syndrome: Impact of Autologous Hematopoietic Stem Cell Transplantation". Archives of Dermatology. 146 (6). doi:10.1001/archdermatol.2010.100. ISSN 0003-987X.
  13. Hara, Daisuke; et al. (2017-10). "Utility of osteosclerotic lesion biopsy in diagnosis of POEMS syndrome: A case report". Medicine. 96 (41): e8188. doi:10.1097/MD.0000000000008188. ISSN 1536-5964. PMC 5662307. PMID 29019884. Check date values in: |date= (help)
  14. 14.0 14.1 Dispenzieri, Angela (2012-06-14). "How I treat POEMS syndrome". Blood. 119 (24): 5650–5658. doi:10.1182/blood-2012-03-378992. ISSN 0006-4971. PMC 3425020. PMID 22547581.CS1 maint: PMC format (link)
  15. Dao, Linda N.; et al. (2011-06-16). "Bone marrow histopathology in POEMS syndrome: a distinctive combination of plasma cell, lymphoid, and myeloid findings in 87 patients". Blood. 117 (24): 6438–6444. doi:10.1182/blood-2010-11-316935. ISSN 0006-4971. PMC 3123015. PMID 21385854.CS1 maint: PMC format (link)
  16. Kang, Wen-Ying; et al. (2013-12). "14q32 translocations and 13q14 deletions are common cytogenetic abnormalities in POEMS syndrome". European Journal of Haematology. 91 (6): 490–496. doi:10.1111/ejh.12189. Check date values in: |date= (help)
  17. Nagao, Yuhei; et al. (2019-07). "Genetic and transcriptional landscape of plasma cells in POEMS syndrome". Leukemia. 33 (7): 1723–1735. doi:10.1038/s41375-018-0348-x. ISSN 1476-5551. Check date values in: |date= (help)
  18. 18.0 18.1 Lin, Qingqing; et al. (2020-06-01). "Somatic Mutations Confer Severe Peripheral Neuropathy in POEMS Syndrome-Associated Multicentric Castleman Disease". Neuroscience Bulletin. 36 (6): 664–666. doi:10.1007/s12264-020-00481-y. ISSN 1995-8218. PMC PMC7270242 Check |pmc= value (help). PMID 32166648 Check |pmid= value (help).CS1 maint: PMC format (link)
  19. Gherardi, R. K.; et al. (1996-02-15). "Overproduction of proinflammatory cytokines imbalanced by their antagonists in POEMS syndrome". Blood. 87 (4): 1458–1465. ISSN 0006-4971. PMID 8608236.
  20. "POEMS syndrome - Symptoms and causes".
  21. "Guillain-Barré syndrome". 2017-10-23.
  22. 22.0 22.1 22.2 Shi, Xiaofeng; et al. (2015-01). "Clinicopathologic Analysis of POEMS Syndrome and Related Diseases". Clinical Lymphoma Myeloma and Leukemia. 15 (1): e15–e21. doi:10.1016/j.clml.2014.04.017. ISSN 2152-2650. Check date values in: |date= (help)
  23. Nozza, Andrea (2017-09-01). "POEMS SYNDROME: AN UPDATE". Mediterranean Journal of Hematology and Infectious Diseases. 9 (1): e2017051. doi:10.4084/MJHID.2017.051. ISSN 2035-3006.

Notes

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*Citation of this Page: “Plasma cell neoplasms with associated paraneoplastic syndrome”. Compendium of Cancer Genome Aberrations (CCGA), Cancer Genomics Consortium (CGC), updated 09/6/2024, https://ccga.io/index.php/HAEM5:Plasma_cell_neoplasms_with_associated_paraneoplastic_syndrome.