vitiligo

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vitiligo overview causes diagnosis treatment American Academy of Dermatology

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clinical photograph vitiligo sharply demarcated depigmented patches

Clinical photography of axillary skin showing depigmented vitiligo patches. Modality: Clinical photograph, dermoscopy not used. The image depicts a large, well-demarcated, chalk-white macule/patch centered in the axillary fold with irregular but sharply defined borders. Adjacent skin exhibits relative hyperpigmentation surrounding the patch, consistent with repigmentation margins typical of vitiligo-affected areas. The surface appears smooth, non-scaly, and non-erythematous, with no crusting or ulceration. Hair within the depigmented areas may be reduced or absent, although follicular retention can occur. Lesions are unilateral and localized to the axilla in this view; a second smaller depigmented area is visible nearby. The clinical impression is consistent with localized vitiligo (leukoderma) presenting as hypopigmented to depigmented patches due to melanocyte destruction. The absence of scale distinguishes vitiligo from tinea versicolor or eczema; the uniform whiteness under standard lighting supports vitiligo rather than postinflammatory hypopigmentation. This image is relevant for educational descriptions of vitiligo morphology, differential diagnosis (hypopigmentation variants, pityriasis versicolor), and for demonstrating axillary involvement. Potential clinical utility includes patient counseling, Wood lamp correlation, and monitoring treatment response to topical corticosteroids, calcineurin inhibitors, or phototherapy over time. Image serves as a reference for clinicians evaluating depigmented lesions and educating patients about prognosis.

Clinical photography of axillary skin showing depigmented vitiligo patches. Modality: Clinical photograph, dermoscopy not used. The image depicts a large, well-demarcated, chalk-white macule/patch centered in the axillary fold with irregular but sharply defined borders. Adjacent skin exhibits relative hyperpigmentation surrounding the patch, consistent with repigmentation margins typical of vitiligo-affected areas. The surface appears smooth, non-scaly, and non-erythematous, with no crusting or ulceration. Hair within the depigmented areas may be reduced or absent, although follicular retention can occur. Lesions are unilateral and localized to the axilla in this view; a second smaller depigmented area is visible nearby. The clinical impression is consistent with localized vitiligo (leukoderma) presenting as hypopigmented to depigmented patches due to melanocyte destruction. The absence of scale distinguishes vitiligo from tinea versicolor or eczema; the uniform whiteness under standard lighting supports vitiligo rather than postinflammatory hypopigmentation. This image is relevant for educational descriptions of vitiligo morphology, differential diagnosis (hypopigmentation variants, pityriasis versicolor), and for demonstrating axillary involvement. Potential clinical utility includes patient counseling, Wood lamp correlation, and monitoring treatment response to topical corticosteroids, calcineurin inhibitors, or phototherapy over time. Image serves as a reference for clinicians evaluating depigmented lesions and educating patients about prognosis.

Clinical photograph of a pediatric patient with generalized vitiligo and secondary skin changes. The image displays extensive, sharply demarcated patches of depigmentation (achromia) on the forehead, chest, and lower lip, contrasting with the patient's natural dark skin tone. Notable leukotrichia (depigmented hair) is visible on the scalp. Within the larger depigmented macules on the forehead and upper chest, there are superimposed erythematous erosions, hemorrhagic crusting, and dark brown scabs, likely representing secondary cutaneous damage, such as actinic injury or superinfection in the unprotected amelanotic skin. The distribution is multi-focal, involving the face and trunk. This case illustrates the clinical presentation of early-onset vitiligo and the vulnerability of depigmented skin to environmental or secondary factors in a young child with a family history of the condition.

Clinical photograph of a pediatric patient with generalized vitiligo and secondary skin changes. The image displays extensive, sharply demarcated patches of depigmentation (achromia) on the forehead, chest, and lower lip, contrasting with the patient's natural dark skin tone. Notable leukotrichia (depigmented hair) is visible on the scalp. Within the larger depigmented macules on the forehead and upper chest, there are superimposed erythematous erosions, hemorrhagic crusting, and dark brown scabs, likely representing secondary cutaneous damage, such as actinic injury or superinfection in the unprotected amelanotic skin. The distribution is multi-focal, involving the face and trunk. This case illustrates the clinical presentation of early-onset vitiligo and the vulnerability of depigmented skin to environmental or secondary factors in a young child with a family history of the condition.

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Vitiligo

Vitiligo is an acquired condition in which the skin loses pigment because pigment-producing cells, called melanocytes, are lost. It causes well-defined white or milky-white patches of skin, sometimes with white hairs within the affected area. It is not contagious and is not caused by poor hygiene. Dermatology 2-Volume Set, 5e, p. 1307.
Vitiligo: sharply defined depigmented patch

Why it happens

Vitiligo involves genetic susceptibility and an immune process that damages melanocytes. It can occur at any age and affects people of every skin tone. It may be associated with autoimmune conditions, particularly thyroid disease. Dermatology 2-Volume Set, 5e, p. 1307. See the AAD overview.

Patterns

  • Non-segmental vitiligo: patches on multiple body areas, often symmetrically, and may progress intermittently.
  • Segmental vitiligo: typically limited to one side or region of the body and often stabilizes after an initial period.

Diagnosis

A dermatologist usually diagnoses it by examining the skin, often with a Wood lamp. They may consider blood tests, especially thyroid testing, if symptoms or history suggest an associated autoimmune disease.

Treatment

There is no guaranteed permanent cure, but many people can slow progression or regain some color. Options depend on location, extent, age, and whether it is active:
  • Sun protection with broad-spectrum SPF 30+ to prevent burns and reduce contrast
  • Cosmetic camouflage or self-tanner
  • Prescription topical treatments, such as corticosteroids, calcineurin inhibitors, or ruxolitinib cream in appropriate patients
  • Narrowband UVB phototherapy for more extensive disease
  • Excimer laser/light for selected localized patches
  • Surgical grafting or cell-based procedures for stable, treatment-resistant localized disease
Dermatology references advise stopping or reconsidering topical treatment if there is no visible improvement after several months, under clinician supervision. Dermatology 2-Volume Set, 5e, p. 1307. The AAD treatment guide outlines these options.

When to seek evaluation

Arrange a dermatology visit if new white patches are appearing, spreading, affecting the face/genitals, or causing distress. Seek prompt assessment if the spots are scaly, itchy, painful, or inflamed, since those features can indicate a different diagnosis, such as fungal infection or eczema.

Kidney stone

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nephrolithiasis prevention

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kidney stones symptoms when to seek emergency help diagnosis treatment prevention NIDDK

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diagram kidney stone in ureter urinary tract obstruction

Kidney stone

A kidney stone is a hard crystal that forms from minerals in the urine. Stones may remain in the kidney or move into the ureter, the tube draining urine to the bladder. A stone in the ureter can cause severe, wave-like pain called renal colic. Brenner and Rector's The Kidney, 2-Volume Set, Urolithiasis section.

Common symptoms

  • Sudden, severe pain in the side, back, lower abdomen, or groin
  • Pain that comes in waves
  • Nausea or vomiting
  • Blood in urine, or cloudy/foul-smelling urine
  • Burning or urgency when urinating
The NIDDK symptom guide describes these typical features.

Seek urgent medical care today if you have

  • Fever, chills, or feel unwell with flank/back pain
  • Severe or uncontrolled pain
  • Vomiting or inability to keep fluids down
  • Trouble passing urine or very little urine
  • A single kidney, pregnancy, known kidney disease, or immunosuppression
A blocked infected kidney is an emergency and may need immediate drainage plus antibiotics.

How it is diagnosed

Clinicians use a urine test, blood tests when needed, and imaging. Non-contrast CT is commonly used in adults; ultrasound may be preferred in pregnancy or when minimizing radiation. If you pass a stone, save it in a clean container or strainer for analysis. Imaging such as ultrasound or CT can identify a stone, as described by the Urology Care Foundation.

Treatment

Treatment depends on stone size, location, pain, infection, and kidney obstruction:
  • Small stones: pain control, anti-nausea medication, fluids as tolerated, and time to pass it. Some patients may be prescribed a medicine to relax the ureter.
  • Large, obstructing, infected, or persistent stones: urology procedures such as shock-wave lithotripsy, ureteroscopy with laser fragmentation, or occasionally percutaneous removal.
The NIDDK treatment overview notes that stones causing obstruction, severe pain, or dehydration can require urgent treatment.

Reducing future stones

For most people, the main prevention measure is sufficient water intake to keep urine pale yellow. Avoiding excessive salt intake, maintaining normal dietary calcium rather than eliminating calcium, and tailoring diet or medicines to the stone type are often important. Recurrent stone formers may need a 24-hour urine test and stone analysis.
Recent evidence: a 2026 systematic review on prevention of recurrent nephrolithiasis is indexed in PubMed (PMID 41871357).

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Could you clarify what you mean by “??”
If you meant you have symptoms possibly due to a kidney stone, tell me:
  • Where the pain is and when it started
  • Whether you have fever/chills, vomiting, blood in urine, or trouble urinating
  • Your age and whether you are pregnant or have one kidney/kidney disease
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ureteral calculi hydronephrosis management

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ureteral stone hydronephrosis emergency fever urine obstruction urology care foundation

Your ultrasound shows stones in both kidneys, with the more urgent issue on the right side:

Main findings

  1. Right ureteric stone
    • A 6.4 mm stone at the right UVJ, where the ureter joins the bladder.
    • It is causing mild hydronephrosis and hydroureter, meaning urine is backing up and dilating the right kidney and ureter.
    • There are also a few small 2-3 mm stones in the right kidney.
  2. Left kidney stone
    • A 7 mm stone in the mid calyx of the left kidney.
    • It is causing minimal focal caliectasis, a small amount of dilation in part of the kidney.
    • There are also a few small 2-3 mm stones in the left kidney.
  3. Gallbladder
    • A tiny 3 mm possible gallbladder polyp. It is not described as a mobile gallstone and has no shadowing.
    • This is usually monitored with repeat ultrasound as advised by your clinician.
  4. Otherwise
    • Liver, spleen, visible pancreas, prostate, and bladder appear broadly normal.
    • No abdominal fluid or pleural fluid seen.

What needs to happen

Because the right-sided 6.4 mm UVJ stone is obstructing urine flow, arrange a urologist consultation promptly, ideally today or within 24-48 hours. A non-contrast CT KUB is commonly used to confirm exact stone size and location and guide treatment. Your doctor may request:
  • Urine routine and culture
  • Kidney function tests: creatinine, urea, electrolytes
  • CBC if infection is possible
  • Stone analysis if you pass a stone
Some stones around this size may pass with pain medication and a ureter-relaxing medicine prescribed by a clinician, but others need a procedure such as ureteroscopy/laser treatment or temporary stenting. Ultrasound can show dilation but CT better confirms the obstructing stone. National Kidney Foundation Primer on Kidney Diseases, 8e, Obstructive Uropathy section.

Go to emergency care now if you have

  • Fever or chills
  • Severe or worsening pain not controlled with medication
  • Repeated vomiting or inability to drink fluids
  • Very low urine output or inability to pass urine
  • Weakness, confusion, or feeling very unwell
Fever or infection with an obstructed kidney is a urological emergency because it may need urgent drainage. The NIDDK kidney stone guidance also advises urgent evaluation for stones causing obstruction, severe pain, or dehydration.
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