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Chromoblastomycosis

Updated : June 22, 2022





Background

The symptoms of chromoblastomycosis are slow-growing, cauliflower-like lesions that could ulcerate, and these lesions are caused by a variety of brown pigment-producing dematiaceous fungi. The fungi develop solitary or multicellular clusters with thick walls.

These fungi find their way into the body through trauma, and lesions are consequently more prevalent on exposed body parts. The condition is chronic, but the vast majority of cases are curable.

Epidemiology

The regions most affected by this condition are the tropics and the subtropics. Individuals working in the agricultural field have a greater tendency to be affected, especially males.

Although rarer, children are also affected by chromoblastomycosis. Most of the world has reported cases of this disease, including Madagascar, Northern Europe, North, Central and South America, Jamaica, Cuba, and Australia.

Anatomy

Pathophysiology

After the skin suffers trauma, the fungi find their way into the skin and evoke a granulomatous response. Following this, the epidermis displays pseudoepitheliomatous hyperplasia, and a granuloma made of Langerhans giant cells and epithelioid cells is seen in the dermis.

The final elements can be seen as sclerotic bodies. As chromoblastomycosis manifests itself, black dots are seen on the surface of the lesion; they are extruded transepidermally.

Etiology

Numerous fungi are capable of causing the sickness. They are dematiaceous, meaning that they produce brown pigment.

Some of the most prevalent fungi which cause this disease include:

  • Phialophora verrucosa
  • Fonsecea pedrosoi
  • Cladosporium carrionii
  • Other fungi which are slightly less common are:
  • Exophialia spinier
  • Fonsacea compactum
  • Wangiella dermatitidis
  • Exophialia jeanselmei
  • Rhinocladiella aquaspersa

As a result of trauma, the fungi enter the body from wood and dirt. This illness is prevalent in rural areas. Cladosporium carrionii reproduces via fission.

It generates numerous conidia in long, straight chains that emerge from the hyphae, with the youngest conidia located furthest from the hyphae.

Genetics

Prognostic Factors

Chromoblastomycosis can be be completely cured through effective treatment. If it’s detected in the early stages, the prognosis is generally favourable, and there is a smaller chance of long-lasting symptoms.

Cases which have spread to the joints and are involved with the lymphatic system have a high chance of morbidity.

Once the illness has spread to the CNS, the prognosis is highly unfavorable. Individuals who have small lesions have a swift recovery after surgery, followed by anti-fungal therapy.

Clinical History

Physical Examination

Age group

Associated comorbidity

Associated activity

Acuity of presentation

Differential Diagnoses

Laboratory Studies

Imaging Studies

Procedures

Histologic Findings

Staging

Treatment Paradigm

by Stage

by Modality

Chemotherapy

Radiation Therapy

Surgical Interventions

Hormone Therapy

Immunotherapy

Hyperthermia

Photodynamic Therapy

Stem Cell Transplant

Targeted Therapy

Palliative Care

Medication

Media Gallary

References

https://www.ncbi.nlm.nih.gov/books/NBK470253/

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Chromoblastomycosis

Updated : June 22, 2022




The symptoms of chromoblastomycosis are slow-growing, cauliflower-like lesions that could ulcerate, and these lesions are caused by a variety of brown pigment-producing dematiaceous fungi. The fungi develop solitary or multicellular clusters with thick walls.

These fungi find their way into the body through trauma, and lesions are consequently more prevalent on exposed body parts. The condition is chronic, but the vast majority of cases are curable.

The regions most affected by this condition are the tropics and the subtropics. Individuals working in the agricultural field have a greater tendency to be affected, especially males.

Although rarer, children are also affected by chromoblastomycosis. Most of the world has reported cases of this disease, including Madagascar, Northern Europe, North, Central and South America, Jamaica, Cuba, and Australia.

After the skin suffers trauma, the fungi find their way into the skin and evoke a granulomatous response. Following this, the epidermis displays pseudoepitheliomatous hyperplasia, and a granuloma made of Langerhans giant cells and epithelioid cells is seen in the dermis.

The final elements can be seen as sclerotic bodies. As chromoblastomycosis manifests itself, black dots are seen on the surface of the lesion; they are extruded transepidermally.

Numerous fungi are capable of causing the sickness. They are dematiaceous, meaning that they produce brown pigment.

Some of the most prevalent fungi which cause this disease include:

  • Phialophora verrucosa
  • Fonsecea pedrosoi
  • Cladosporium carrionii
  • Other fungi which are slightly less common are:
  • Exophialia spinier
  • Fonsacea compactum
  • Wangiella dermatitidis
  • Exophialia jeanselmei
  • Rhinocladiella aquaspersa

As a result of trauma, the fungi enter the body from wood and dirt. This illness is prevalent in rural areas. Cladosporium carrionii reproduces via fission.

It generates numerous conidia in long, straight chains that emerge from the hyphae, with the youngest conidia located furthest from the hyphae.

Chromoblastomycosis can be be completely cured through effective treatment. If it’s detected in the early stages, the prognosis is generally favourable, and there is a smaller chance of long-lasting symptoms.

Cases which have spread to the joints and are involved with the lymphatic system have a high chance of morbidity.

Once the illness has spread to the CNS, the prognosis is highly unfavorable. Individuals who have small lesions have a swift recovery after surgery, followed by anti-fungal therapy.

https://www.ncbi.nlm.nih.gov/books/NBK470253/

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