Anagen Effluvium Workup

  • Author: Robert A Schwartz, MD, MPH; Chief Editor: Dirk M Elston, MD   more...
 
Updated: Mar 9, 2012
 

Laboratory Studies

A few select laboratory studies may be performed, as indicated by features of the history or physical findings. Serologic tests may include the following:

  • Iron studies
  • Thyroid function tests[11]
  • Rapid plasma reagin (RPR) and Venereal Disease Research Laboratory (VDRL) tests
  • Antinuclear antibody (ANA) tests

Serum and urine amino acid levels may be determined.

If tinea capitis is a concern in the differential diagnosis, microscopic examination for fungal elements and culture for fungi may be performed.[12]

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Other Tests

Phototrichography, trichoscanning, trichoscopy, and reflectance confocal microscopy may be used to evaluate hair loss from anagen effluvium.[13]

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Procedures

Anagen effluvium can be distinguished from telogen effluvium by means of the pull test. To perform this test, firmly grasping 40 hairs between the thumb and forefinger and slowly pull on them to remove them, causing only mild discomfort to the patient. Then, a trichogram is used to quantify the ratio of terminal anagen hairs to telogen hairs. Anagen and telogen hairs can often be identified with the naked eye, but any doubts can be resolved by means of light microscopy. Anagen hairs have long indented roots covered with intact inner and outer root sheaths, and they are fully pigmented. Telogen hairs have short, club-shaped roots. They lack root sheaths and show depigmentation of the proximal part of the shaft. Fewer than 4-6 telogen hairs are typically present. A greater number of telogen hairs indicates a shift toward the telogen phase and suggests a probable diagnosis of telogen effluvium.

An alternative to is perform a gentle pull test or examine hairs removed by combing. The presence of tapered fractures is diagnostic of anagen effluvium.

Anagen effluvium can be distinguished from other forms of alopecia on the basis of the histologic changes on horizontal sections. A 4-mm punch biopsy sample of the scalp contains 25-50 follicles for inspection. Less than 15% of the follicles are normally in the telogen phase. A normal anagen-to-telogen ratio in a patient with hair loss is characteristic of anagen effluvium. A finding of greater than 15% of follicles in the telogen phase indicates a significant shift toward telogen in most individuals. This finding suggests telogen effluvium. The follicles should show no signs of inflammation, dystrophic changes of the inner sheath, or traction. These features permit the distinction of anagen effluvium from alopecia areata, androgenetic alopecia, and traction alopecia.

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Histologic Findings

Anagen hairs have long, indented roots covered with intact inner and outer root sheaths. These hairs are fully pigmented. Telogen hairs have short, club-shaped roots. These hairs lack root sheaths and show depigmentation of the proximal parts of the shaft.

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Contributor Information and Disclosures
Author

Robert A Schwartz, MD, MPH  Professor and Head, Dermatology, Professor of Pathology, Pediatrics, Medicine, and Preventive Medicine and Community Health, University of Medicine and Dentistry of New Jersey-New Jersey Medical School

Robert A Schwartz, MD, MPH is a member of the following medical societies: Alpha Omega Alpha, American Academy of Dermatology, American College of Physicians, and Sigma Xi

Disclosure: Nothing to disclose.

Coauthor(s)

Bryan D Seiff, MD  Staff Physician, Department of Ophthalmology, NY Presbyterian Hospital-Cornell

Bryan D Seiff, MD is a member of the following medical societies: Alpha Omega Alpha

Disclosure: Nothing to disclose.

Pere Gascon, MD, PhD  Professor and Director, Division of Medical Oncology, Institute of Hematology and Medical Oncology, IDIBAPS, University of Barcelona Faculty of Medicine, Spain

Pere Gascon, MD, PhD is a member of the following medical societies: Alpha Omega Alpha, American College of Physicians, New York Academy of Medicine, New York Academy of Sciences, and Sigma Xi

Disclosure: Nothing to disclose.

Specialty Editor Board

Günter Burg, MD  Professor and Chairman Emeritus, Department of Dermatology, University of Zürich School of Medicine; Delegate of The Foundation for Modern Teaching and Learning in Medicine Faculty of Medicine, University of Zürich, Switzerland

Günter Burg, MD is a member of the following medical societies: American Academy of Dermatology, American Dermatological Association, International Society for Dermatologic Surgery, North American Clinical Dermatologic Society, and Pacific Dermatologic Association

Disclosure: Nothing to disclose.

David F Butler, MD  Professor of Dermatology, Texas A&M University College of Medicine; Chair, Department of Dermatology, Director, Dermatology Residency Training Program, Scott and White Clinic, Northside Clinic

David F Butler, MD is a member of the following medical societies: Alpha Omega Alpha, American Academy of Dermatology, American Medical Association, American Society for Dermatologic Surgery, American Society for MOHS Surgery, Association of Military Dermatologists, and Phi Beta Kappa

Disclosure: Nothing to disclose.

Rosalie Elenitsas, MD  Herman Beerman Associate Professor of Dermatology, University of Pennsylvania School of Medicine; Director, Penn Cutaneous Pathology Services, Department of Dermatology, University of Pennsylvania Health System

Rosalie Elenitsas, MD is a member of the following medical societies: American Academy of Dermatology and American Society of Dermatopathology

Disclosure: Lippincott Williams Wilkins Royalty Textbook editor; DLA Piper Consulting fee Consulting

Catherine M Quirk, MD  Clinical Assistant Professor, Department of Dermatology, University of Pennsylvania

Catherine M Quirk, MD is a member of the following medical societies: Alpha Omega Alpha and American Academy of Dermatology

Disclosure: Nothing to disclose.

Chief Editor

Dirk M Elston, MD  Director, Ackerman Academy of Dermatopathology, New York

Dirk M Elston, MD is a member of the following medical societies: American Academy of Dermatology

Disclosure: Nothing to disclose.

References
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  2. Trueb RM. Chemotherapy-induced alopecia. Semin Cutan Med Surg. Mar 2009;28(1):11-4. [Medline].

  3. Delmonte S, Semino MT, Parodi A, Rebora A. Normal anagen effluvium: a sign of pemphigus vulgaris. Br J Dermatol. Jun 2000;142(6):1244-5. [Medline].

  4. Bronner AK, Hood AF. Cutaneous complications of chemotherapeutic agents. J Am Acad Dermatol. Nov 1983;9(5):645-63. [Medline].

  5. Tosi A, Misciali C, Piraccini BM, Peluso AM, Bardazzi F. Drug-induced hair loss and hair growth. Incidence, management and avoidance. Drug Saf. Apr 1994;10(4):310-7. [Medline].

  6. Tosti A, Pazzaglia M. Drug reactions affecting hair: diagnosis. Dermatol Clin. Apr 2007;25(2):223-31. [Medline].

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  8. Tallon B, Blanchard E, Goldberg LJ. Permanent chemotherapy-induced alopecia: Case report and review of the literature. J Am Acad Dermatol. May 12 2010;[Medline].

  9. Miteva M, Misciali C, Fanti PA, Vincenzi C, Romanelli P, Tosti A. Permanent Alopecia After Systemic Chemotherapy: A Clinicopathological Study of 10 Cases. Am J Dermatopathol. Mar 11 2011;[Medline].

  10. Quercetani R, Rebora AE, Fedi MC, Carelli G, Mei S, Chelli A, et al. Patients with profuse hair shedding may reveal anagen hair dystrophy: a diagnostic clue of alopecia areata incognita. J Eur Acad Dermatol Venereol. Jul 2011;25(7):808-10. [Medline].

  11. van Beek N, Bodo E, Kromminga A, et al. Thyroid hormones directly alter human hair follicle functions: anagen prolongation and stimulation of both hair matrix keratinocyte proliferation and hair pigmentation. J Clin Endocrinol Metab. Nov 2008;93(11):4381-8. [Medline].

  12. Trovato MJ, Schwartz RA, Janniger CK. Tinea capitis: current concepts in clinical practice. Cutis. Feb 2006;77(2):93-9. [Medline].

  13. Olszewska M, Warszawik O, Rakowska A, Slowinska M, Rudnicka L. [Methods of hair loss evaluation in patients with endocrine disorders]. Endokrynol Pol. 2011;62 Suppl 1:29-34. [Medline].

  14. Duvic M, Lemak NA, Valero V, Hymes SR, et al. A randomized trial of minoxidil in chemotherapy-induced alopecia. J Am Acad Dermatol. Jul 1996;35(1):74-8. [Medline].

  15. Merial-Kieny C, Nocera T, Mery S. [Medical corrective make-up in post- chemotherapy]. Ann Dermatol Venereol. Jan 2008;Spec No 1:25-8. [Medline].

  16. [Guideline] University of Texas at Austin, School of Nursing, Family Nurse Practitioner Program. Recommendations to diagnose and treat adult hair loss disorders or alopecia in primary care settings (non pregnant female and male adults). National Guidelines Clearinghouse. May 2004;[Full Text].

  17. Jimenez JJ, Roberts SM, Mejia J, et al. Prevention of chemotherapy-induced alopecia in rodent models. Cell Stress Chaperones. Spring 2008;13(1):31-8. [Medline].

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