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  In this article
   Abstract
   Introduction
   History
   Nuclear warfare
   Biological warfare
   Conclusion
   References
   Article Figures
   Article Tables

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REVIEW ARTICLE
Year : 2005  |  Volume : 71  |  Issue : 2  |  Page : 80-86

Cutaneous reactions in nuclear, biological and chemical warfare


Skin Centre, Base Hospital, Delhi, India

Correspondence Address:
Sandeep Arora
Skin Centre, Base Hospital, Delhi Cantt - 110 010
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0378-6323.13989

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  Abstract 

Nuclear, biological and chemical warfare have in recent times been responsible for an increasing number of otherwise rare dermatoses. Many nations are now maintaining overt and clandestine stockpiles of such arsenal. With increasing terrorist threats, these agents of mass destruction pose a risk to the civilian population. Nuclear and chemical attacks manifest immediately while biological attacks manifest later. Chemical and biological attacks pose a significant risk to the attending medical personnel. The large scale of anticipated casualties in the event of such an occurrence would need the expertise of all physicians, including dermatologists, both military and civilian. Dermatologists are uniquely qualified in this respect. This article aims at presenting a review of the cutaneous manifestations in nuclear, chemical and biological warfare and their management.


Keywords: Nuclear warfare, Biological warfare, Chemical warfare, Cutaneous manifestations


How to cite this article:
Arora S. Cutaneous reactions in nuclear, biological and chemical warfare. Indian J Dermatol Venereol Leprol 2005;71:80-6

How to cite this URL:
Arora S. Cutaneous reactions in nuclear, biological and chemical warfare. Indian J Dermatol Venereol Leprol [serial online] 2005 [cited 2019 Nov 13];71:80-6. Available from: http://www.ijdvl.com/text.asp?2005/71/2/80/13989



  Introduction Top




It is the constant endeavor of warring enemies to use new technologies and means in an attempt to gain advantage.[1],[2],[3] This article aims at increasing awareness among dermatologists of the specific cutaneous manifestations of agents of neclear, biological and chemical (NBC) warfare [Table - 1], [Table - 2].[4] Civilians may encounter these agents during a terrorist or military attack, a riot control operation, or due to accidental exposure during industrial or agricultural use. Military personnel may be exposed during their active use in the battlefield or exposure to areas where the disease may be chronically endemic.




  History Top




Some weapons not only inflict casualties but manage to strike considerable fear in the enemy. It is the unique blend of real and perceived danger that makes nuclear, biological, and chemical weapons so appealing. Nuclear warfare historically dates back to the bombing of Nagasaki and Hiroshima in 1945. Dr. Michihiko Achiya's diary clearly describes the evolution of radiation symptoms and the constellation of signs associated with radiation poisoning.[5]



The earliest mention of biological warfare is found on an Assyrian tablet dated from 600 BC which refers to a noxious pustule in the ear of grains. Biological warfare attacks took place at the Black Sea port of Kaffa (now Feodossia, Ukraine) in 1346. Other examples are the 'yellow rain' (trichothecene mycotoxins) attacks in Southeast Asia between 1974 and 1981; the weaponization of anthrax, botulinum toxin, and aflatoxin;[6] and the release of sarin nerve gas in a Japanese subway in 1995 by the Aum Shinrikyo cult.[3] Other examples include the use of arsenical smoke as early as 1000 BC by the Chinese, mustard gas by Egypt against Yemen, Agent Orange (a defoliant) during the Vietnam War, and more recently, vesicants (blistering agents, e.g. mustard gas) and nerve gas by Iraq.[7]




  Nuclear warfare Top




The cutaneous effects of a nuclear explosion are always due to one of three effects: blast injuries (direct and indirect), thermal burns, and radiation injuries. The majority of energy from a nuclear device is blast and thermal energy, the same energy released from a conventional bomb.[8]



Thermal burns can be caused directly by the initial explosion or by fires that are secondary to it. Ionizing radiation, comprising charged alpha and beta particles, can only penetrate the skin, causing an initial erythema that can progress to superficial and deep ulcers. Conversely, gamma rays, X-rays, and neutrons, all of which have no charge, penetrate deeply into the body and can cause severe damage to vital tissues. Further cutaneous damage depends upon the extent of radiation exposure [Table - 3]. Individuals exposed to ionizing radiation need long term follow up.[9]



Skin biopsy reveals keratinocyte damage with pyknotic nuclei, severe dermal edema, and subepidermal vesicle formation. With higher doses, endothelial cell swelling, intravascular thrombi, and fibrosis can be seen. Patient contamination poses little risk to medical personnel and should not hinder appropriate lifesaving measures in an emergency. Management includes decontamination and wound care. For decontamination, soap and water, normal saline or povidone iodine and water can be used. Wound care is similar to that for burns. Sulfhydryl drugs, pentoxifylline and recently topical tazarotene[10] have beneficial effects.




  Biological warfare Top




Biological warfare (BW) is defined as the 'employment of biological agents to produce casualties in man or animals or damage to plants.' These agents are highly virulent, produce severe illness and are usually resistant to common modes of treatment. They are particularly attractive as they can be aerosolized, and reach the lower respiratory tract. A list of such agents and their management are mentioned in [Table - 2] and [Table - 4].[11],[12],[13],[14],[15],[16]



Anthrax



Anthrax is primarily a zoonotic disease caused by Bacillus anthracis that produces a toxin consisting of a protective antigen, edema factor and a lethal factor. The WHO estimates that 50 kg of anthrax spores released upwind in a population center of 500,000 could result in up to 95,000 deaths, with a further 125,000 people incapacitated.[17]



When the skin is the portal of entry, the earliest finding is that of a pruritic macule that progresses through papular, vesicular, or pustular stages to an ulcer with a blackened, necrotic eschar and surrounding nonpitting, gelatinous, and painless edema on an exposed surface. Satellite vesicles and painful regional lymphadenitis are other features. Systemic features are usually absent, but septic shock and severe edema can occur.



Diagnosis is based on gram stain, cultures or direct immunofluorescence. Anthrax toxin may be detected in the blood by immunoassays. Organisms can be demonstrated from a full thickness skin biopsy done from periphery of a vesicle or eschar. However, the absence of organisms in the biopsy specimen does not rule out anthrax. Specific management [Table - 3] includes ciprofloxacin and doxycycline. In 2001, adsorbed anthrax vaccine was used in the United States in combination with post-exposure prophylaxis (PEP).



Plague



Because of its high mortality (approximately 200 million deaths throughout history), Yersinia pestis has attracted attention for development as a possible BW agent. On inoculation 4-10% individuals may develop a pustule at the inoculation site.[18] Terminal pneumonic and septicemic plague patients would develop livid cyanosis and large ecchymoses on the back. Septicemia could cause petechiae, purpura, ecchymoses, and acral cyanosis and necrosis leading to the infamous description, 'the Black Death.' Cases of ecthyma gangrenosum-like lesions and carbuncles due to plague have been reported.[19]



Investigations include bubo aspiration for direct microscopy, and culture on blood agar of bubo aspirate, cerebrospinal fluid, blood and sputum. Isolation of patients for a minimum of 72 hours after detection and accompanying the administration of antibiotics [Table - 3] is recommended. PEP must be adopted in those exposed but not manifesting the clinical features and the medical personnel involved in the management. An outbreak of endemic plague is heralded by affection of the mammalian reservoirs first while a BW attack would first affect the humans.



Tularemia



Tularemia is a zoonosis caused by Francisella tularensis. The commoner forms include the ulceroglandular form, which involves the skin and lymph nodes, and the typhoidal form. A cutaneous ulcer occurs in approximately 60% of patients and is the most common sign of tularemia.[20] Ulcers are generally single lesions of 0.4 to 3.0 cm in diameter, with heaped-up edges and accompanied with systemic upset. The organism is difficult to culture; hence the diagnosis is usually established by serology.[21] A live, attenuated vaccine is effective against aerosol infection.[20]



Melioidosis



Burkholderia (formerly Pseudomonas) pseudomallei is a gram-negative bacillus. Cutaneous manifestations include severe urticaria,[22] flushing and cyanosis. Inhalational melioidosis could lead to pustules or cutaneous abscesses associated with lymphangitis, cellulitis, or regional lymphadenitis, but only after metastatic abscesses to the skin are formed, and this would be likely to take months.[23]



Viral hemorrhagic fevers



Hemorrhagic fever viruses, with the exception of dengue, are potentially transmitted via aerosol. Cutaneous manifestations are non-specific and include flushing, petechiae, purpura, ecchymoses, and edema.



ELISA to detect specific IgM antibody responses must be done. One should not wait for viral cultures, which consume time, to initiate management [Table - 3]. Management includes supportive care for prevention of hypotension and shock. Medical personnel need to be protected. Isolation of the patient during active disease and strict barrier nursing must be adopted. Specific treatment may include ribavirin. Only yellow fever has a licensed vaccine.[24]



Other viral fevers



The viral species important from the warfare context include variola (smallpox), monkeypox, and vaccinia. Smallpox has an incubation period of 7-17 days and a prodrome of 2-4 days. An enanthem on the buccal and pharyngeal mucosa starts on about the second day. An orderly progress of macules to papules, vesicles, pustules (sometimes umbilicated), and crusts distributed in a centrifugal pattern (in distinction to varicella) over a 1-2 week period is typical. Crusts are infective and detach in about 3 weeks leaving depressed, hypopigmented scars. Monkeypox greatly resembles variola, the only distinguishing feature being cervical and inguinal lymphadenopathy.



Trichothecene mycotoxins



Trichothecene mycotoxins ('Yellow rain')[25] are the only potential BW toxins with cutaneous activity and manifestations. Mycotoxins are a diverse group of small molecular weight compounds produced by the fungi of five fungal genera: Aspergillus, Penicillium, Fusarium, Alternaria, and Claviceps. 'Yellow rain' was used in Southeast Asia between 1974 and 1981. Most attacks used yellow pigment, but some used red, green, white, or brown smoke or vapor. Vesication often occurred with 'yellow rain' attacks. At low doses (nanograms), severe skin irritation with erythema, edema, and necrosis is observed.



A mask and full-body clothing are protective. The clothing gear and contaminated areas of skin should be washed with soap and water followed by a water rinse. Washing within 4-6 hours of exposure removes 80-98% of the toxin and prevents death and dermal lesions in experimental animals. High doses of systemic steroids decrease toxin injury.



Chemical warfare



A chemical warfare (CW) agent is a chemical substance, gaseous, liquid or solid, which might be employed because of its direct toxic effects on man, animals and plants.



The intention of chemical warfare is to reduce the enemy's numbers by increasing the morbidity. These agents are manmade, volatile, dermally active and act primarily on the skin, eyes and the upper respiratory tract.



The general management in all suspected CW attacks includes decontamination with adequate protection of the attending medical personnel. Skin protection against chemical weapons is provided by special protective clothing which may either be impermeable to liquids or which is permeable to air and moisture but has been treated to prevent chemical weapons agents from getting through. Individual protective equipment, as used by certain armies, includes special clothing, gas masks, and antidotes such as atropine and Fuller's earth (which absorbs the liquid CW agents).



Vesicants



Vesicants were used widely in World War I and have been a dreaded threat in every war fought since then. They include the deadly trio of mustards, arsenicals and phosgene oximes.



Mustards



Mustards derive their name from their color, smell and taste which are similar to mustard. They are highly toxic in low concentrations to all organ systems. Clinical manifestations usually occur after four to six hours. In a follow up of 34,000 Iranians over a 13-20 year period, Khateri et al noticed skin involvement in 24.5% [Figure - 1].[7] Skin manifestations include tenderness with dusky erythema or painless sunburn and hyperpigmentation involving both exposed and unexposed parts. Parts of the body where the skin is tender and well supplied with sweat glands are more severely affected. Itching and burning may be present. The fully developed bulla is thin walled and yellowish with surrounding erythema. At the end of twenty-four hours the typical appearance includes progressive, painful, virtually blinding conjunctivitis with constant rhinorrhea and a blistered face; the systemic symptoms include intellectual dullness or stupidity, headache, malaise and exhaustion. Cutaneous healing, with or without scarring, takes days to months.



Biopsy shows hydropic degeneration of basal cells and a split at the level of lamina lucida. No specific antidote exists for mustard. Management includes personal protection, decontamination of the patient, and burns after care. Topical preparations to ameliorate the effects are albumin, collagen, powdered milk, gel or collagen dressings, activated charcoal slurry (for inactivation), ice bags (to cool the skin), trichloroacetic acid crystal application,[26] vitamin E and niacin.



Arsenical vesicants



Chlorovinyldichloroarsine, or Lewisite, is an arsenical vesicant. Lewisite acts like mustard but does not cause immunosuppression. Other differences include earlier onset of pain (within seconds to minutes of exposure), a decreased incidence of skin infection, and a shorter healing time (2-3 weeks). Topical application of British anti-Lewisite (BAL) ointment within 5 minutes of exposure and an intramuscular injection of the same may decrease some of the epidermal and systemic toxicity of Lewisite.



Halogenated oximes



Phosgene oxime (CX) belongs to a class of chemical agents called urticants or nettle gases. It penetrates rubber and garments much more easily. Phosgene oxime is not a true vesicant, but it is extremely irritating to the epidermal and mucosal tissues. Immediate irritation and burning similar to stinging nettle is followed by urticaria like edema, and blistering after 24 hours. The skin can become necrotic, and healing may take 3 months or even longer. Specific treatment consists of immediate decontamination with water and sodium bicarbonate solution.



Nerve agents and cyanides



Five organophosphorous compounds are generally regarded as nerve agents [Table - 1].



Nerve agents inhibit cholinesterase which then cannot hydrolyze acetyl choline. They differ from common organophosphorous agents by being much more toxic. The cutaneous effects of nerve agents are mostly limited to the areas of exposure. Increased sweating and goose bumps and fasciculations secondary to the muscarinic-like effect of the agents on eccrine sweat gland innervation and arrector pilori are evident. Tabun and sarin cause cyanotic redness and edema of the skin respectively. Treatment of nerve agents consists of the administration of atropine followed by pralidoxime chloride to reactivate acetylcholinesterase.



The cyanides (blood agents) act by inactivating cytochrome oxidase, preventing cellular oxygen utilization. The blood remains oxygenated and the mucosal membranes and skin of an affected individual appear dark red. The only effective therapy is amyl nitrite inhalation followed by sodium thiosulfate.



Riot control agents



Agents used in riot control [Table - 1] are primarily lacrimators, sternutators and vomiting agents. Cutaneous reactions are secondary and not the primary intentional event. After an initial burning sensation, erythema develops and persists for an hour or so. However continual or large exposure results in intense erythema and vesiculation. Initial exposure may later be followed by an allergic contact dermatitis.[27] Dermatological management is as for any dermatitis. Sodium hypochlorite (household bleach) is useful in the management.



The threat of chemical warfare is ever real and all dermatologists must be prepared to treat a large number of affected individuals if such an event occurs. The fact that medical personnel need to adopt adequate protection, follow strict decontamination procedures and triage during administration of treatment is what differentiates these casualties from ordinary accidents involving these chemicals.




  Conclusion Top




The primary threat from chemical and biological agents today is from terrorists. Civilians in densely populated regions are the likely targets. Therefore, both civilian and military dermatologists need to be aware of how a biological, chemical or nuclear attack would present, to minimize its effects. Dermatologists can play a role in recognizing the early markers of an attack and in its management.

 
  References Top

1.Update: Investigation of bio terrorism-related anthrax: Connecticut, 2001. MMWR Morb Mortal Wkly Rep 2001;50:1077-9.  Back to cited text no. 1      
2.Torok TJ, Tauxe RF, Wise RP, Livengood JR, Sokolow R, Mauvais S, et al. A large community outbreak of salmonellosis caused by intentional contamination of restaurant salad bars. JAMA 1997;278:389-95.  Back to cited text no. 2      
3.Okumura T, Takasu N, Ishimatasu S, Miyanoki S, Mitsuhashi A, Kumada K, et al. Report on 640 victims of the Tokyo subway sarin attack. Ann Emerg Med 1996;28:129-35.   Back to cited text no. 3      
4.Rotz LD, Khan AS, Lillibridge SR, Ostroff SM, Hughes JM. Public health assessment of potential biological terrorism agents. Emerg Infect Dis 2002;8:225-30.  Back to cited text no. 4  [PUBMED]  [FULLTEXT]  
5.Achiya M, Wells W, Trans. The Journal of a Japanese Physician, August 6-September 30, 1945, Hiroshima Diary. Chapel Hill, NC: University of North Carolina Press; 1955. p. 14-5.  Back to cited text no. 5      
6.Witkowski JA, Parish LC. The story of anthrax from antiquity to the present: A biological weapon of nature and humans. Clin Dermatol 2002;20:336-42.  Back to cited text no. 6  [PUBMED]  [FULLTEXT]  
7.Khateri S, Ghanei M, Keshavarz S, Soroush M, Haines D. Incidence of lung, eye, and skin lesions as late complications in 34,000 Iranians with wartime exposure to mustard agent. J Occup Environ Med 2003;45:1136-43.  Back to cited text no. 7  [PUBMED]  [FULLTEXT]  
8.Nuclear warfare. Effects of a nuclear explosion. Available at: http://en.wikipedia.org/wiki/Nuclear_weapon.htm. Accessed 7 Aug. 2004.  Back to cited text no. 8      
9.Steinert M, Weiss M, Gottlober P, Belyi D, Gergel O, Bebeshko V, et al. Delayed effects of accidental cutaneous radiation exposure: Fifteen years of follow-up after the Chernobyl accident. J Am Acad Dermatol 2003;49:417-23.  Back to cited text no. 9  [PUBMED]  [FULLTEXT]  
10.So PL, Lee K, Hebert J, Walker P, Lu Y, Hwang J, et al. Topical tazarotene chemoprevention reduces Basal cell carcinoma number and size in Ptch1+/- mice exposed to ultraviolet or ionizing radiation. Cancer Res 2004;64:4385-9.  Back to cited text no. 10  [PUBMED]  [FULLTEXT]  
11.Polyak CS, Macy JT, Irizarry-De La Cruz M, Lai JE, McAuliffe JF, Popovic T, et al. Bioterrorism-related anthrax: International response by the Centers for Disease Control and Prevention. Emerg Infect Dis 2002;8:1056-9.  Back to cited text no. 11  [PUBMED]  [FULLTEXT]  
12.Inglesby TV, Henderson DA, Bartlett JG, Ascher MS, Eitzen E, Friedlander AM, et al. Anthrax as a biological weapon: medical and public health management Working Group on Civilian Biodefense. JAMA 1999;281:1735-45.  Back to cited text no. 12  [PUBMED]  [FULLTEXT]  
13.Henderson DA, Inglesby TV, Bartlett JG, Ascher MS, Eitzen E, Jahrling PB, et al. Smallpox as a biological weapon: Medical and public health management Working Group on Civilian Biodefense. JAMA 1999;281:2127-37.  Back to cited text no. 13  [PUBMED]  [FULLTEXT]  
14.Inglesby TV, Dennis DT, Henderson DA, Bartlett JG, Ascher MS, Eitzen E, et al. Plague as a biological weapon: Medical and public health management. Working Group on Civilian Biodefense. JAMA 2000;283:2281-90.  Back to cited text no. 14  [PUBMED]  [FULLTEXT]  
15.Arnon SS, Schechter R, Inglesby TV, Henderson DA, Bartlett JG, Ascher MS, et al. Botulinum toxin as a biological weapon: medical and public health management. JAMA 2001;285:1059-70.  Back to cited text no. 15  [PUBMED]  [FULLTEXT]  
16.Inglesby TV, O'Toole T, Henderson DA, Bartlett JG, Ascher MS, Eitzen E, et al. Anthrax as a biological weapon, 2002: Updated recommendations for management. JAMA 2002;287:2236-52.  Back to cited text no. 16      
17.Huxsoll DL, Parrott CD, Patrick WC 3rd. Medicine in defense against biological warfare. JAMA 1989;262:677-9.  Back to cited text no. 17  [PUBMED]    
18.Crook LD, Tempest B. Plague: A clinical review of 27 cases. Arch Intern Med 1992;152:1253-6.  Back to cited text no. 18  [PUBMED]    
19.Welty TK, Grabman J, Kompare E, Wood G, Welty E, Van Duzen J, et al. Nineteen cases of plague in Arizona: A spectrum including ecthyma gangrenosum due to plague and plague in pregnancy. West J Med 1985;42:641-6.  Back to cited text no. 19      
20.Friedlander AM, Evans ME, Tularemia. In: Sidell FR, Takafuji ET, Franz DR, editors. Textbook of military medicine: Medical aspects of chemical and biological warfare, part 1. Washington (DC): Walter Reed Army Medical Center; 1997. p. 503-12.  Back to cited text no. 20      
21.Centers for Disease Control and Prevention. Basic laboratory protocols for the presumptive identification of Francisella tularensis. Available at: http://www.bt.cdc.gov/Agent/Tularemia/tularemia20010417.pdf. accessed on 7 Aug, 2004.  Back to cited text no. 21      
22.Steck WD, Byrd RB. Urticaria secondary to pulmonary melioidosis. Report of a case. Arch Dermatol 1969;99:80-1.  Back to cited text no. 22  [PUBMED]    
23.Wuthiekanun V, Amornchai P, Chierakul W, Cheng AC, White NJ, Peacock SJ, et al. Evaluation of Immunoglobulin M (IgM) and IgG Rapid Cassette Test Kits for Diagnosis of Melioidosis in an Area of Endemicity. J Clin Microbiol 2004;42:3435-7.  Back to cited text no. 23  [PUBMED]  [FULLTEXT]  
24.Barrett AD. Current status of the Arilvax; yellow fever vaccine. Expert Rev Vaccines 2004;3:413-20.  Back to cited text no. 24  [PUBMED]  [FULLTEXT]  
25.Seely TD, Nowicke JW, Meselson M, Guillemin J, Akratanakkul P. Yellow rain. Sci Am 1985;253:128-37.  Back to cited text no. 25      
26.Papirmeister B, Feister AJ, Robinson SI, Ford RD. Medical Defense against Mustard Gas, Toxic Mechanisms and Pharmacological Implications. Boston, Mass: CRC Press; 1991. p. 80-2.  Back to cited text no. 26      
27.Holland P, White RG. The cutaneous reactions produced by o-chlorobenzylidene malononitrile and 1- chloroacetophenone when applied directly to the skin of human subjects. Br J Dermatol 1972;86:150-4.  Back to cited text no. 27  [PUBMED]    


    Figures

  [Figure - 1]
 
 
    Tables

  [Table - 1], [Table - 2], [Table - 3], [Table - 4]

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